rs876657396

Orientation

plus

Stabilized

plus

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

Make rs876657396(C;G)

Make rs876657396(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

40089416

Gene

THRA

is a	snp
is	mentioned by
dbSNP	rs876657396
dbSNP (classic)	rs876657396
ClinGen	rs876657396
ebi	rs876657396
HLI	rs876657396
Exac	rs876657396
Gnomad	rs876657396
Varsome	rs876657396
LitVar	rs876657396
Map	rs876657396
PheGenI	rs876657396
Biobank	rs876657396
1000 genomes	rs876657396
hgdp	rs876657396
ensembl	rs876657396
geneview	rs876657396
scholar	rs876657396
google	rs876657396
pharmgkb	rs876657396
gwascentral	rs876657396
openSNP	rs876657396
23andMe	rs876657396
SNPshot	rs876657396
SNPdbe	rs876657396
MSV3d	rs876657396
GWAS Ctlg	rs876657396

Max Magnitude

0

ClinVar
Risk	rs876657396(G;G)
Alt	rs876657396(G;G)
Reference	Rs876657396(C;C)
Significance	Pathogenic
Disease	Hypothyroidism
Variation	info
Gene	THRA
CLNDBN	Hypothyroidism, congenital, nongoitrous, 6
Reversed	0
HGVS	NC_000017.10:g.38245669C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000172855.3,