rs121909666

Orientation

plus

Stabilized

plus

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

Make rs121909666(A;A)

Make rs121909666(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

30233692

Gene	FSHB, LOC105376607

is a	snp
is	mentioned by
dbSNP	rs121909666
dbSNP (classic)	rs121909666
ClinGen	rs121909666
ebi	rs121909666
HLI	rs121909666
Exac	rs121909666
Gnomad	rs121909666
Varsome	rs121909666
LitVar	rs121909666
Map	rs121909666
PheGenI	rs121909666
Biobank	rs121909666
1000 genomes	rs121909666
hgdp	rs121909666
ensembl	rs121909666
geneview	rs121909666
scholar	rs121909666
google	rs121909666
pharmgkb	rs121909666
gwascentral	rs121909666
openSNP	rs121909666
23andMe	rs121909666
SNPshot	rs121909666
SNPdbe	rs121909666
MSV3d	rs121909666
GWAS Ctlg	rs121909666

Max Magnitude

0

OMIM	136530
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909666(A;A)
Alt	rs121909666(A;A)
Reference	Rs121909666(C;C)
Significance	Pathogenic
Disease	Follicle-stimulating hormone deficiency
Variation	info
Gene	FSHB
CLNDBN	Follicle-stimulating hormone deficiency, isolated
Reversed	0
HGVS	NC_000011.9:g.30255239C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017629.28,