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rs16904774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs16904774(A;A)
Make rs16904774(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position132888250
GeneTG
is asnp
is mentioned by
dbSNPrs16904774
dbSNP (old)rs16904774
ClinGenrs16904774
ebirs16904774
HLIrs16904774
Exacrs16904774
Gnomadrs16904774
Varsomers16904774
Maprs16904774
PheGenIrs16904774
Biobankrs16904774
1000 genomesrs16904774
hgdprs16904774
ensemblrs16904774
gopubmedrs16904774
geneviewrs16904774
scholarrs16904774
googlers16904774
pharmgkbrs16904774
gwascentralrs16904774
openSNPrs16904774
23andMers16904774
23andMe allrs16904774
SNPshotrs16904774
SNPdbers16904774
MSV3drs16904774
GWAS Ctlgrs16904774
Max Magnitude0
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs16904774(A;A) rs16904774(T;T)
Alt rs16904774(A;A) rs16904774(T;T)
Reference Rs16904774(G;G)
Significance Pathogenic
Disease Thyroid dyshormonogenesis not provided
Variation info
Gene TG
CLNDBN Thyroid dyshormonogenesis not provided
Reversed 0
HGVS NC_000008.10:g.133900495G>A; NC_000008.10:g.133900495G>T
CLNSRC
CLNACC RCV000388671.1, RCV000412820.1,