{{Rsnum
|rsid=1670533
|Gene=RNF212
|Chromosome=4
|position=1084399
|Orientation=minus
|GMAF=0.2332
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=RNF212
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 27.4 | 64.6
| HCB | 11.7 | 43.1 | 45.3
| JPT | 15.9 | 58.4 | 25.7
| YRI | 0.0 | 4.1 | 95.9
| ASW | 0.0 | 14.0 | 86.0
| CHB | 11.7 | 43.1 | 45.3
| CHD | 15.6 | 42.2 | 42.2
| GIH | 5.0 | 32.7 | 62.4
| LWK | 0.0 | 9.1 | 90.9
| MEX | 19.0 | 32.8 | 48.3
| MKK | 0.0 | 13.5 | 86.5
| TSI | 5.9 | 42.2 | 52.0
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs1670533
|PubMedID=18239089
|Condition=Recombination rate (females)
|Gene=RNF212,SPON2
|Risk Allele=C
|pValue=2.00E-012
|OR=88.2
|95CI=63.7-112.7) cM increas
}}

{{omim
|desc=RECOMBINATION RATE QUANTITATIVE TRAIT LOCUS 1; RRQTL1
|id=612042
|rsnum=1670533
}}

{{omim
|id=612041
|desc=RING FINGER PROTEIN 212; RNF212
|rsnum=1670533
}}

{{PharmGKB
|RSID=rs1670533
|Name_s=
|Gene_s=RNF212
|Feature=
|Evidence=PubMed ID:18239089; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS Results: Sequence Variants in the RNF212 Gene Associate with Genomewide Recombination Rate (Initial Sample Size: 1,702 women; Replication Sample Size: 1,663 women; Risk Allele: rs1670533-C).
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356736
}}

{{PharmGKB
|RSID=rs1670533
|Name_s=
|Gene_s=RNF212
|Feature=
|Evidence=PubMed ID:18239089
|Annotation=This SNP is correlated with genome-wide recombination rate;opposite effects are observed in males and females.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Curated
|PharmGKB Accession ID=PA161410653
}}

{{omim
|id=612041
|rsnum=1670533
|variant=0001
}}

{{omim
|id=612041
|rsnum=1670533
|variant=0002
}}

{{PMID Auto
|PMID=19002143
|Title=Sex-specific genetic architecture of human disease.
|OA=1
}}

{{PMID Auto
|PMID=19763160
|Title=Genetic analysis of variation in human meiotic recombination.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1670533
|overall_frequency_n=104
|overall_frequency_d=126
|overall_frequency=0.825397
|n_genomes=52
|n_genomes_annotated=0
|n_haplomes=88
|n_articles=1
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}