rs121909662

Orientation

minus

Stabilized

minus

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

Make rs121909662(A;A)

Make rs121909662(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48963266

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs121909662
dbSNP (classic)	rs121909662
ClinGen	rs121909662
ebi	rs121909662
HLI	rs121909662
Exac	rs121909662
Gnomad	rs121909662
Varsome	rs121909662
LitVar	rs121909662
Map	rs121909662
PheGenI	rs121909662
Biobank	rs121909662
1000 genomes	rs121909662
hgdp	rs121909662
ensembl	rs121909662
geneview	rs121909662
scholar	rs121909662
google	rs121909662
pharmgkb	rs121909662
gwascentral	rs121909662
openSNP	rs121909662
23andMe	rs121909662
SNPshot	rs121909662
SNPdbe	rs121909662
MSV3d	rs121909662
GWAS Ctlg	rs121909662

Max Magnitude

0

OMIM	136435
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121909662(A;A)
Alt	rs121909662(A;A)
Reference	Rs121909662(C;C)
Significance	Pathogenic
Disease	Ovarian dysgenesis 1
Variation	info
Gene	FSHR
CLNDBN	Ovarian dysgenesis 1
Reversed	1
HGVS	NC_000002.11:g.49190405G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017639.23,