rs121909663

Orientation

minus

Stabilized

minus

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

Make rs121909663(A;G)

Make rs121909663(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48963476

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs121909663
dbSNP (classic)	rs121909663
ClinGen	rs121909663
ebi	rs121909663
HLI	rs121909663
Exac	rs121909663
Gnomad	rs121909663
Varsome	rs121909663
LitVar	rs121909663
Map	rs121909663
PheGenI	rs121909663
Biobank	rs121909663
1000 genomes	rs121909663
hgdp	rs121909663
ensembl	rs121909663
geneview	rs121909663
scholar	rs121909663
google	rs121909663
pharmgkb	rs121909663
gwascentral	rs121909663
openSNP	rs121909663
23andMe	rs121909663
SNPshot	rs121909663
SNPdbe	rs121909663
MSV3d	rs121909663
GWAS Ctlg	rs121909663

Max Magnitude

0

OMIM	136435
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121909663(G;G)
Alt	rs121909663(G;G)
Reference	Rs121909663(A;A)
Significance	Pathogenic
Disease	Ovarian hyperstimulation syndrome
Variation	info
Gene	FSHR
CLNDBN	Ovarian hyperstimulation syndrome
Reversed	1
HGVS	NC_000002.11:g.49190615T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017640.28,