{{Rsnum
|rsid=35211634
|Gene=GIF
|Chromosome=11
|position=59845386
|Orientation=plus
|GMAF=0.08494
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=GIF
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 10.6 | 88.5
| HCB | 0.0 | 2.9 | 97.1
| JPT | 0.0 | 7.1 | 92.9
| YRI | 4.1 | 27.9 | 68.0
| ASW | 0.0 | 35.1 | 64.9
| CHB | 0.0 | 2.9 | 97.1
| CHD | 0.9 | 8.3 | 90.8
| GIH | 0.0 | 5.9 | 94.1
| LWK | 3.6 | 48.2 | 48.2
| MEX | 0.0 | 1.7 | 98.3
| MKK | 9.6 | 34.0 | 56.4
| TSI | 0.0 | 1.0 | 99.0
| HapMapRevision=28
}}{{omim
|id=609342
|rsnum=35211634
|variant=0001
}}

{{ClinVar
|rsid=35211634
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=59612859
|CHROM=11
|GMAF=0.0847
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x05016000000015051f110100
|GENEINFO=GIF:2694
|GENE_NAME=GIF
|GENE_ID=2694
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.59612859T>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9151; 0.08494
|CLNACC=RCV000001812.1
|CLNDBN=Intrinsic factor deficiency, congenital, susceptibility to
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=609342.0001
|COMMON=1
|Disease=Intrinsic factor deficiency
}}

{{GET Evidence
|gene=GIF
|aa_change=Gln23Arg
|aa_change_short=Q23R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs35211634
|overall_frequency_n=1064
|overall_frequency_d=10758
|overall_frequency=0.0989031
|n_genomes=9
|n_genomes_annotated=0
|n_haplomes=11
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.003
|nblosum100=0
|autoscore=1
|n_web_uneval=10
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}