rs121908879

Orientation

plus

Stabilized

plus

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

Make rs121908879(A;G)

Make rs121908879(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81096641

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908879
dbSNP (classic)	rs121908879
ClinGen	rs121908879
ebi	rs121908879
HLI	rs121908879
Exac	rs121908879
Gnomad	rs121908879
Varsome	rs121908879
LitVar	rs121908879
Map	rs121908879
PheGenI	rs121908879
Biobank	rs121908879
1000 genomes	rs121908879
hgdp	rs121908879
ensembl	rs121908879
geneview	rs121908879
scholar	rs121908879
google	rs121908879
pharmgkb	rs121908879
gwascentral	rs121908879
openSNP	rs121908879
23andMe	rs121908879
SNPshot	rs121908879
SNPdbe	rs121908879
MSV3d	rs121908879
GWAS Ctlg	rs121908879

Max Magnitude

0

OMIM	603372
Desc
Variant	0024
Related	also

ClinVar
Risk	rs121908879(G;G)
Alt	rs121908879(G;G)
Reference	Rs121908879(A;A)
Significance	Pathogenic
Disease	Hyperthyroidism
Variation	info
Gene	LOC101928462 TSHR
CLNDBN	Hyperthyroidism, familial gestational
Reversed	0
HGVS	NC_000014.8:g.81562985A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006824.2,