rs121909659

Orientation

minus

Stabilized

minus

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

Make rs121909659(C;C)

Make rs121909659(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48989022

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs121909659
dbSNP (classic)	rs121909659
ClinGen	rs121909659
ebi	rs121909659
HLI	rs121909659
Exac	rs121909659
Gnomad	rs121909659
Varsome	rs121909659
LitVar	rs121909659
Map	rs121909659
PheGenI	rs121909659
Biobank	rs121909659
1000 genomes	rs121909659
hgdp	rs121909659
ensembl	rs121909659
geneview	rs121909659
scholar	rs121909659
google	rs121909659
pharmgkb	rs121909659
gwascentral	rs121909659
openSNP	rs121909659
23andMe	rs121909659
SNPshot	rs121909659
SNPdbe	rs121909659
MSV3d	rs121909659
GWAS Ctlg	rs121909659

Max Magnitude

0

OMIM	136435
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909659(C;C)
Alt	rs121909659(C;C)
Reference	Rs121909659(T;T)
Significance	Pathogenic
Disease	Ovarian dysgenesis 1 not provided
Variation	info
Gene	FSHR
CLNDBN	Ovarian dysgenesis 1 not provided
Reversed	1
HGVS	NC_000002.11:g.49216161A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017631.24, RCV000431545.1,