rs587777871

Orientation

minus

Stabilized

minus

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

Make rs587777871(C;C)

Make rs587777871(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

118827925

Gene

MCM9

is a	snp
is	mentioned by
dbSNP	rs587777871
dbSNP (classic)	rs587777871
ClinGen	rs587777871
ebi	rs587777871
HLI	rs587777871
Exac	rs587777871
Gnomad	rs587777871
Varsome	rs587777871
LitVar	rs587777871
Map	rs587777871
PheGenI	rs587777871
Biobank	rs587777871
1000 genomes	rs587777871
hgdp	rs587777871
ensembl	rs587777871
geneview	rs587777871
scholar	rs587777871
google	rs587777871
pharmgkb	rs587777871
gwascentral	rs587777871
openSNP	rs587777871
23andMe	rs587777871
SNPshot	rs587777871
SNPdbe	rs587777871
MSV3d	rs587777871
GWAS Ctlg	rs587777871

Max Magnitude

0

ClinVar
Risk	rs587777871(C;C)
Alt	rs587777871(C;C)
Reference	Rs587777871(T;T)
Significance	Pathogenic
Disease	Premature ovarian failure 1 Ovarian dysgenesis 4
Variation	info
Gene	MCM9
CLNDBN	Premature ovarian failure 1 Ovarian dysgenesis 4
Reversed	1
HGVS	NC_000006.11:g.119149088A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144731.1, RCV000149815.4,