rs121908862

Orientation

plus

Stabilized

plus

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

Make rs121908862(A;A)

Make rs121908862(A;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81092563

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908862
dbSNP (classic)	rs121908862
ClinGen	rs121908862
ebi	rs121908862
HLI	rs121908862
Exac	rs121908862
Gnomad	rs121908862
Varsome	rs121908862
LitVar	rs121908862
Map	rs121908862
PheGenI	rs121908862
Biobank	rs121908862
1000 genomes	rs121908862
hgdp	rs121908862
ensembl	rs121908862
geneview	rs121908862
scholar	rs121908862
google	rs121908862
pharmgkb	rs121908862
gwascentral	rs121908862
openSNP	rs121908862
23andMe	rs121908862
SNPshot	rs121908862
SNPdbe	rs121908862
MSV3d	rs121908862
GWAS Ctlg	rs121908862

Max Magnitude

0

OMIM	603372
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121908862(A;A)
Alt	rs121908862(A;A)
Reference	Rs121908862(T;T)
Significance	Pathogenic
Disease	Hypothyroidism
Variation	info
Gene	LOC101928462 TSHR
CLNDBN	Hypothyroidism, congenital, nongoitrous, 1
Reversed	0
HGVS	NC_000014.8:g.81558907T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006804.3,