rs587777872

Orientation

minus

Stabilized

minus

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

Make rs587777872(C;T)

Make rs587777872(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

118924038

Gene

MCM9

is a	snp
is	mentioned by
dbSNP	rs587777872
dbSNP (classic)	rs587777872
ClinGen	rs587777872
ebi	rs587777872
HLI	rs587777872
Exac	rs587777872
Gnomad	rs587777872
Varsome	rs587777872
LitVar	rs587777872
Map	rs587777872
PheGenI	rs587777872
Biobank	rs587777872
1000 genomes	rs587777872
hgdp	rs587777872
ensembl	rs587777872
geneview	rs587777872
scholar	rs587777872
google	rs587777872
pharmgkb	rs587777872
gwascentral	rs587777872
openSNP	rs587777872
23andMe	rs587777872
SNPshot	rs587777872
SNPdbe	rs587777872
MSV3d	rs587777872
GWAS Ctlg	rs587777872

Max Magnitude

0

ClinVar
Risk	rs587777872(T;T)
Alt	rs587777872(T;T)
Reference	Rs587777872(C;C)
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.119245203G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144732.1, RCV000149816.4,