rs121909660

Orientation

minus

Stabilized

minus

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

Make rs121909660(C;T)

Make rs121909660(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48963104

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs121909660
dbSNP (classic)	rs121909660
ClinGen	rs121909660
ebi	rs121909660
HLI	rs121909660
Exac	rs121909660
Gnomad	rs121909660
Varsome	rs121909660
LitVar	rs121909660
Map	rs121909660
PheGenI	rs121909660
Biobank	rs121909660
1000 genomes	rs121909660
hgdp	rs121909660
ensembl	rs121909660
geneview	rs121909660
scholar	rs121909660
google	rs121909660
pharmgkb	rs121909660
gwascentral	rs121909660
openSNP	rs121909660
23andMe	rs121909660
SNPshot	rs121909660
SNPdbe	rs121909660
MSV3d	rs121909660
GWAS Ctlg	rs121909660

Max Magnitude

0

OMIM	136435
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121909660(T;T)
Alt	rs121909660(T;T)
Reference	Rs121909660(C;C)
Significance	Pathogenic
Disease	Ovarian dysgenesis 1
Variation	info
Gene	FSHR
CLNDBN	Ovarian dysgenesis 1
Reversed	1
HGVS	NC_000002.11:g.49190243G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017632.29,