rs121918670

Orientation

plus

Stabilized

plus

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

Make rs121918670(C;T)

Make rs121918670(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

115034015

Gene

TSHB

is a	snp
is	mentioned by
dbSNP	rs121918670
dbSNP (classic)	rs121918670
ClinGen	rs121918670
ebi	rs121918670
HLI	rs121918670
Exac	rs121918670
Gnomad	rs121918670
Varsome	rs121918670
LitVar	rs121918670
Map	rs121918670
PheGenI	rs121918670
Biobank	rs121918670
1000 genomes	rs121918670
hgdp	rs121918670
ensembl	rs121918670
geneview	rs121918670
scholar	rs121918670
google	rs121918670
pharmgkb	rs121918670
gwascentral	rs121918670
openSNP	rs121918670
23andMe	rs121918670
SNPshot	rs121918670
SNPdbe	rs121918670
MSV3d	rs121918670
GWAS Ctlg	rs121918670

Max Magnitude

0

OMIM	188540
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121918670(T;T)
Alt	rs121918670(T;T)
Reference	Rs121918670(C;C)
Significance	Pathogenic
Disease	Secondary hypothyroidism
Variation	info
Gene	TSHB
CLNDBN	Secondary hypothyroidism
Reversed	0
HGVS	NC_000001.10:g.115576636C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013524.22,