rs121908876

Orientation

plus

Stabilized

plus

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

Make rs121908876(A;A)

Make rs121908876(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143572

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908876
dbSNP (classic)	rs121908876
ClinGen	rs121908876
ebi	rs121908876
HLI	rs121908876
Exac	rs121908876
Gnomad	rs121908876
Varsome	rs121908876
LitVar	rs121908876
Map	rs121908876
PheGenI	rs121908876
Biobank	rs121908876
1000 genomes	rs121908876
hgdp	rs121908876
ensembl	rs121908876
geneview	rs121908876
scholar	rs121908876
google	rs121908876
pharmgkb	rs121908876
gwascentral	rs121908876
openSNP	rs121908876
23andMe	rs121908876
SNPshot	rs121908876
SNPdbe	rs121908876
MSV3d	rs121908876
GWAS Ctlg	rs121908876

Max Magnitude

0

OMIM	603372
Desc
Variant	0021
Related	also

ClinVar
Risk	rs121908876(A;A)
Alt	rs121908876(A;A)
Reference	Rs121908876(G;G)
Significance	Pathogenic
Disease	Hyperthyroidism
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hyperthyroidism, nonautoimmune
Reversed	0
HGVS	NC_000014.8:g.81609916G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006820.2,