{{Rsnum
|rsid=2076740
|Gene=TG
|Chromosome=8
|position=132971813
|Orientation=plus
|GMAF=0.3301
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TG
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 36.3 | 50.4 | 13.3
| HCB | 65.7 | 29.9 | 4.4
| JPT | 64.6 | 31.9 | 3.5
| YRI | 19.7 | 44.2 | 36.1
| ASW | 38.6 | 38.6 | 22.8
| CHB | 65.7 | 29.9 | 4.4
| CHD | 61.5 | 33.9 | 4.6
| GIH | 56.4 | 39.6 | 4.0
| LWK | 29.1 | 52.7 | 18.2
| MEX | 51.7 | 39.7 | 8.6
| MKK | 21.8 | 46.8 | 31.4
| TSI | 41.2 | 46.1 | 12.7
| HapMapRevision=28
}}
{{omim
|id=188450
|variant=0008
|rsnum=2076740
}}
{{PMID Auto
|PMID=22265031
|Title=Epistasis between the HSD17B4 and TG polymorphisms is associated with premature ovarian failure
}}{{ClinVar
|rsid=2076740
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=133984058
|CHROM=8
|GMAF=0.3301
|dbSNPBuildID=96
|SSR=0
|SAO=1
|VP=0x05016800000017051f110100
|GENEINFO=TG:7038
|GENE_NAME=TG
|GENE_ID=7038
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.133984058C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=188450.0008
|CLNSIG=255
|CLNCUI=C1842444
|CLNDBN=Autoimmune thyroid disease 3
|Disease=Autoimmune thyroid disease 3
|CLNACC=RCV000013533.1
|Tags=PM;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.6699; 0.3301
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1842444:608175
|COMMON=1
}}{{GET Evidence
|gene=TG
|aa_change=Arg1999Trp
|aa_change_short=R1999W
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2076740
|overall_frequency_n=4247
|overall_frequency_d=10758
|overall_frequency=0.394776
|n_genomes=36
|n_genomes_annotated=0
|n_haplomes=48
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=1
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=7
|autoscore=1
|webscore=N
}}