rs28928871

Orientation

minus

Stabilized

minus

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

Make rs28928871(A;A)

Make rs28928871(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48963122

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs28928871
dbSNP (classic)	rs28928871
ClinGen	rs28928871
ebi	rs28928871
HLI	rs28928871
Exac	rs28928871
Gnomad	rs28928871
Varsome	rs28928871
LitVar	rs28928871
Map	rs28928871
PheGenI	rs28928871
Biobank	rs28928871
1000 genomes	rs28928871
hgdp	rs28928871
ensembl	rs28928871
geneview	rs28928871
scholar	rs28928871
google	rs28928871
pharmgkb	rs28928871
gwascentral	rs28928871
openSNP	rs28928871
23andMe	rs28928871
SNPshot	rs28928871
SNPdbe	rs28928871
MSV3d	rs28928871
GWAS Ctlg	rs28928871

Max Magnitude

0

OMIM	136435
Desc	OVARIAN HYPERSTIMULATION SYNDROME
Variant	0009
Related	also

ClinVar
Risk	rs28928871(A;A)
Alt	rs28928871(A;A)
Reference	Rs28928871(G;G)
Significance	Pathogenic
Disease	Ovarian hyperstimulation syndrome
Variation	info
Gene	FSHR
CLNDBN	Ovarian hyperstimulation syndrome
Reversed	1
HGVS	NC_000002.11:g.49190261C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017638.28,