rs121908883

Orientation

plus

Stabilized

plus

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

Make rs121908883(A;A)

Make rs121908883(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143349

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908883
dbSNP (classic)	rs121908883
ClinGen	rs121908883
ebi	rs121908883
HLI	rs121908883
Exac	rs121908883
Gnomad	rs121908883
Varsome	rs121908883
LitVar	rs121908883
Map	rs121908883
PheGenI	rs121908883
Biobank	rs121908883
1000 genomes	rs121908883
hgdp	rs121908883
ensembl	rs121908883
geneview	rs121908883
scholar	rs121908883
google	rs121908883
pharmgkb	rs121908883
gwascentral	rs121908883
openSNP	rs121908883
23andMe	rs121908883
SNPshot	rs121908883
SNPdbe	rs121908883
MSV3d	rs121908883
GWAS Ctlg	rs121908883

Max Magnitude

0

OMIM	603372
Desc
Variant	0028
Related	also

ClinVar
Risk	rs121908883(A;A)
Alt	rs121908883(A;A)
Reference	Rs121908883(G;G)
Significance	Pathogenic
Disease	Hyperthyroidism
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hyperthyroidism, nonautoimmune
Reversed	0
HGVS	NC_000014.8:g.81609693G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006828.2,