rs121908884

Orientation

plus

Stabilized

plus

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

Make rs121908884(C;C)

Make rs121908884(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143856

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908884
dbSNP (classic)	rs121908884
ClinGen	rs121908884
ebi	rs121908884
HLI	rs121908884
Exac	rs121908884
Gnomad	rs121908884
Varsome	rs121908884
LitVar	rs121908884
Map	rs121908884
PheGenI	rs121908884
Biobank	rs121908884
1000 genomes	rs121908884
hgdp	rs121908884
ensembl	rs121908884
geneview	rs121908884
scholar	rs121908884
google	rs121908884
pharmgkb	rs121908884
gwascentral	rs121908884
openSNP	rs121908884
23andMe	rs121908884
SNPshot	rs121908884
SNPdbe	rs121908884
MSV3d	rs121908884
GWAS Ctlg	rs121908884

Max Magnitude

0

OMIM	603372
Desc
Variant	0029
Related	also

ClinVar
Risk	rs121908884(C;C)
Alt	rs121908884(C;C)
Reference	Rs121908884(T;T)
Significance	Pathogenic
Disease	Hypothyroidism
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hypothyroidism, congenital, nongoitrous, 1
Reversed	0
HGVS	NC_000014.8:g.81610200T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006829.3,