rs121909664

Orientation

minus

Stabilized

minus

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

Make rs121909664(C;C)

Make rs121909664(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48963187

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs121909664
dbSNP (classic)	rs121909664
ClinGen	rs121909664
ebi	rs121909664
HLI	rs121909664
Exac	rs121909664
Gnomad	rs121909664
Varsome	rs121909664
LitVar	rs121909664
Map	rs121909664
PheGenI	rs121909664
Biobank	rs121909664
1000 genomes	rs121909664
hgdp	rs121909664
ensembl	rs121909664
geneview	rs121909664
scholar	rs121909664
google	rs121909664
pharmgkb	rs121909664
gwascentral	rs121909664
openSNP	rs121909664
23andMe	rs121909664
SNPshot	rs121909664
SNPdbe	rs121909664
MSV3d	rs121909664
GWAS Ctlg	rs121909664

Max Magnitude

0

OMIM	136435
Desc
Variant	0012
Related	also

ClinVar
Risk	rs121909664(C;C)
Alt	rs121909664(C;C)
Reference	Rs121909664(T;T)
Significance	Pathogenic
Disease	Ovarian hyperstimulation syndrome
Variation	info
Gene	FSHR
CLNDBN	Ovarian hyperstimulation syndrome
Reversed	1
HGVS	NC_000002.11:g.49190326A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017641.28,