rs121908882

Orientation

plus

Stabilized

plus

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

Make rs121908882(C;T)

Make rs121908882(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81142986

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908882
dbSNP (classic)	rs121908882
ClinGen	rs121908882
ebi	rs121908882
HLI	rs121908882
Exac	rs121908882
Gnomad	rs121908882
Varsome	rs121908882
LitVar	rs121908882
Map	rs121908882
PheGenI	rs121908882
Biobank	rs121908882
1000 genomes	rs121908882
hgdp	rs121908882
ensembl	rs121908882
geneview	rs121908882
scholar	rs121908882
google	rs121908882
pharmgkb	rs121908882
gwascentral	rs121908882
openSNP	rs121908882
23andMe	rs121908882
SNPshot	rs121908882
SNPdbe	rs121908882
MSV3d	rs121908882
GWAS Ctlg	rs121908882

Max Magnitude

0

OMIM	603372
Desc
Variant	0027
Related	also

ClinVar
Risk	rs121908882(T;T)
Alt	rs121908882(T;T)
Reference	Rs121908882(C;C)
Significance	Pathogenic
Disease	Hypothyroidism not specified
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hypothyroidism, congenital, nongoitrous, 1 not specified
Reversed	0
HGVS	NC_000014.8:g.81609330C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006827.3, RCV000122250.1,