rs121909658

Orientation

minus

Stabilized

minus

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

Make rs121909658(C;T)

Make rs121909658(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48983125

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs121909658
dbSNP (classic)	rs121909658
ClinGen	rs121909658
ebi	rs121909658
HLI	rs121909658
Exac	rs121909658
Gnomad	rs121909658
Varsome	rs121909658
LitVar	rs121909658
Map	rs121909658
PheGenI	rs121909658
Biobank	rs121909658
1000 genomes	rs121909658
hgdp	rs121909658
ensembl	rs121909658
geneview	rs121909658
scholar	rs121909658
google	rs121909658
pharmgkb	rs121909658
gwascentral	rs121909658
openSNP	rs121909658
23andMe	rs121909658
SNPshot	rs121909658
SNPdbe	rs121909658
MSV3d	rs121909658
GWAS Ctlg	rs121909658

Max Magnitude

0

OMIM	136435
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909658(T;T)
Alt	rs121909658(T;T)
Reference	Rs121909658(C;C)
Significance	Pathogenic
Disease	Ovarian dysgenesis 1
Variation	info
Gene	FSHR
CLNDBN	Ovarian dysgenesis 1
Reversed	1
HGVS	NC_000002.11:g.49210264G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017630.29,