Have questions? Visit https://www.reddit.com/r/SNPedia

rs137853163

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853163(C;C)
Make rs137853163(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position40089333
GeneTHRA
is asnp
is mentioned by
dbSNPrs137853163
ebirs137853163
HLIrs137853163
Exacrs137853163
Varsomers137853163
Maprs137853163
PheGenIrs137853163
hapmaprs137853163
1000 genomesrs137853163
hgdprs137853163
ensemblrs137853163
gopubmedrs137853163
geneviewrs137853163
scholarrs137853163
googlers137853163
pharmgkbrs137853163
gwascentralrs137853163
openSNPrs137853163
23andMers137853163
23andMe allrs137853163
SNP Nexus

SNPshotrs137853163
SNPdbers137853163
MSV3drs137853163
GWAS Ctlgrs137853163
Max Magnitude0
ClinVar
Risk rs137853163(C;C)
Alt rs137853163(C;C)
Reference Rs137853163(G;G)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene THRA
CLNDBN Hypothyroidism, congenital, nongoitrous, 6
Reversed 0
HGVS NC_000017.10:g.38245586G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022801.24,