rs386833511

Orientation

minus

Stabilized

minus

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

Make rs386833511(C;T)

Make rs386833511(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48963097

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs386833511
dbSNP (classic)	rs386833511
ClinGen	rs386833511
ebi	rs386833511
HLI	rs386833511
Exac	rs386833511
Gnomad	rs386833511
Varsome	rs386833511
LitVar	rs386833511
Map	rs386833511
PheGenI	rs386833511
Biobank	rs386833511
1000 genomes	rs386833511
hgdp	rs386833511
ensembl	rs386833511
geneview	rs386833511
scholar	rs386833511
google	rs386833511
pharmgkb	rs386833511
gwascentral	rs386833511
openSNP	rs386833511
23andMe	rs386833511
SNPshot	rs386833511
SNPdbe	rs386833511
MSV3d	rs386833511
GWAS Ctlg	rs386833511

Max Magnitude

0

ClinVar
Risk	rs386833511(T;T)
Alt	rs386833511(T;T)
Reference	Rs386833511(C;C)
Significance	Probable-Pathogenic
Disease	Ovarian dysgenesis 1
Variation	info
Gene	FSHR
CLNDBN	Ovarian dysgenesis 1
Reversed	1
HGVS	NC_000002.11:g.49190236G>A
CLNSRC	ClinVar
CLNACC	RCV000049440.1,

[PMID 20237833] Follicle stimulating hormone receptor gene variants in women with primary and secondary amenorrhea.