rs121908865

Orientation

plus

Stabilized

plus

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

Make rs121908865(A;A)

Make rs121908865(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81087962

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908865
dbSNP (classic)	rs121908865
ClinGen	rs121908865
ebi	rs121908865
HLI	rs121908865
Exac	rs121908865
Gnomad	rs121908865
Varsome	rs121908865
LitVar	rs121908865
Map	rs121908865
PheGenI	rs121908865
Biobank	rs121908865
1000 genomes	rs121908865
hgdp	rs121908865
ensembl	rs121908865
geneview	rs121908865
scholar	rs121908865
google	rs121908865
pharmgkb	rs121908865
gwascentral	rs121908865
openSNP	rs121908865
23andMe	rs121908865
SNPshot	rs121908865
SNPdbe	rs121908865
MSV3d	rs121908865
GWAS Ctlg	rs121908865

Max Magnitude

0

OMIM	603372
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121908865(A;A)
Alt	rs121908865(A;A)
Reference	Rs121908865(G;G)
Significance	Pathogenic
Disease	Hypothyroidism
Variation	info
Gene	LOC101928462 TSHR
CLNDBN	Hypothyroidism, congenital, nongoitrous, 1
Reversed	0
HGVS	NC_000014.8:g.81554306G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006808.3,