rs137853162

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs137853162(G;T)

Make rs137853162(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

40077520

Gene

THRA

is a	snp
is	mentioned by
dbSNP	rs137853162
dbSNP (classic)	rs137853162
ClinGen	rs137853162
ebi	rs137853162
HLI	rs137853162
Exac	rs137853162
Gnomad	rs137853162
Varsome	rs137853162
LitVar	rs137853162
Map	rs137853162
PheGenI	rs137853162
Biobank	rs137853162
1000 genomes	rs137853162
hgdp	rs137853162
ensembl	rs137853162
geneview	rs137853162
scholar	rs137853162
google	rs137853162
pharmgkb	rs137853162
gwascentral	rs137853162
openSNP	rs137853162
23andMe	rs137853162
SNPshot	rs137853162
SNPdbe	rs137853162
MSV3d	rs137853162
GWAS Ctlg	rs137853162

Max Magnitude

0

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,