rs121909661

Orientation

minus

Stabilized

minus

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

Make rs121909661(A;A)

Make rs121909661(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48963566

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs121909661
dbSNP (classic)	rs121909661
ClinGen	rs121909661
ebi	rs121909661
HLI	rs121909661
Exac	rs121909661
Gnomad	rs121909661
Varsome	rs121909661
LitVar	rs121909661
Map	rs121909661
PheGenI	rs121909661
Biobank	rs121909661
1000 genomes	rs121909661
hgdp	rs121909661
ensembl	rs121909661
geneview	rs121909661
scholar	rs121909661
google	rs121909661
pharmgkb	rs121909661
gwascentral	rs121909661
openSNP	rs121909661
23andMe	rs121909661
SNPshot	rs121909661
SNPdbe	rs121909661
MSV3d	rs121909661
GWAS Ctlg	rs121909661

Max Magnitude

0

OMIM	136435
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121909661(A;A)
Alt	rs121909661(A;A)
Reference	Rs121909661(G;G)
Significance	Pathogenic
Disease	Ovarian dysgenesis 1
Variation	info
Gene	FSHR
CLNDBN	Ovarian dysgenesis 1
Reversed	1
HGVS	NC_000002.11:g.49190705C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017636.31,