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rs137853162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853162(G;T)
Make rs137853162(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position40077520
GeneTHRA
is asnp
is mentioned by
dbSNPrs137853162
ebirs137853162
HLIrs137853162
Exacrs137853162
Varsomers137853162
Maprs137853162
PheGenIrs137853162
hapmaprs137853162
1000 genomesrs137853162
hgdprs137853162
ensemblrs137853162
gopubmedrs137853162
geneviewrs137853162
scholarrs137853162
googlers137853162
pharmgkbrs137853162
gwascentralrs137853162
openSNPrs137853162
23andMers137853162
23andMe allrs137853162
SNP Nexus

SNPshotrs137853162
SNPdbers137853162
MSV3drs137853162
GWAS Ctlgrs137853162
Max Magnitude0
ClinVar
Risk rs137853162(T;T)
Alt rs137853162(T;T)
Reference rs137853162(G;G)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene THRA
CLNDBN Hypothyroidism, congenital, nongoitrous, 6
Reversed 0
HGVS NC_000017.10:g.38233773G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022800.24,