rs121908881

Orientation

plus

Stabilized

plus

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

Make rs121908881(C;T)

Make rs121908881(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143488

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908881
dbSNP (classic)	rs121908881
ClinGen	rs121908881
ebi	rs121908881
HLI	rs121908881
Exac	rs121908881
Gnomad	rs121908881
Varsome	rs121908881
LitVar	rs121908881
Map	rs121908881
PheGenI	rs121908881
Biobank	rs121908881
1000 genomes	rs121908881
hgdp	rs121908881
ensembl	rs121908881
geneview	rs121908881
scholar	rs121908881
google	rs121908881
pharmgkb	rs121908881
gwascentral	rs121908881
openSNP	rs121908881
23andMe	rs121908881
SNPshot	rs121908881
SNPdbe	rs121908881
MSV3d	rs121908881
GWAS Ctlg	rs121908881

Max Magnitude

0

OMIM	603372
Desc
Variant	0026
Related	also

ClinVar
Risk	rs121908881(T;T)
Alt	rs121908881(T;T)
Reference	Rs121908881(C;C)
Significance	Pathogenic
Disease	Hypothyroidism
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hypothyroidism, congenital, nongoitrous, 1
Reversed	0
HGVS	NC_000014.8:g.81609832C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006826.3,