rs121908868

Orientation

plus

Stabilized

plus

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

Make rs121908868(A;A)

Make rs121908868(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143286

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908868
dbSNP (classic)	rs121908868
ClinGen	rs121908868
ebi	rs121908868
HLI	rs121908868
Exac	rs121908868
Gnomad	rs121908868
Varsome	rs121908868
LitVar	rs121908868
Map	rs121908868
PheGenI	rs121908868
Biobank	rs121908868
1000 genomes	rs121908868
hgdp	rs121908868
ensembl	rs121908868
geneview	rs121908868
scholar	rs121908868
google	rs121908868
pharmgkb	rs121908868
gwascentral	rs121908868
openSNP	rs121908868
23andMe	rs121908868
SNPshot	rs121908868
SNPdbe	rs121908868
MSV3d	rs121908868
GWAS Ctlg	rs121908868

Max Magnitude

0

OMIM	603372
Desc
Variant	0012
Related	also

ClinVar
Risk	rs121908868(A;A)
Alt	rs121908868(A;A)
Reference	Rs121908868(G;G)
Significance	Pathogenic
Disease	Hypothyroidism
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hypothyroidism, congenital, nongoitrous, 1
Reversed	0
HGVS	NC_000014.8:g.81609630G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006811.4,