rs606231343

Orientation

plus

Stabilized

plus

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

Make rs606231343(C;G)

Make rs606231343(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

20

Position

5955211

Gene

MCM8

is a	snp
is	mentioned by
dbSNP	rs606231343
dbSNP (classic)	rs606231343
ClinGen	rs606231343
ebi	rs606231343
HLI	rs606231343
Exac	rs606231343
Gnomad	rs606231343
Varsome	rs606231343
LitVar	rs606231343
Map	rs606231343
PheGenI	rs606231343
Biobank	rs606231343
1000 genomes	rs606231343
hgdp	rs606231343
ensembl	rs606231343
geneview	rs606231343
scholar	rs606231343
google	rs606231343
pharmgkb	rs606231343
gwascentral	rs606231343
openSNP	rs606231343
23andMe	rs606231343
SNPshot	rs606231343
SNPdbe	rs606231343
MSV3d	rs606231343
GWAS Ctlg	rs606231343

Max Magnitude

0

ClinVar
Risk	rs606231343(G;G)
Alt	rs606231343(G;G)
Reference	Rs606231343(C;C)
Significance	Pathogenic
Disease	not provided Premature ovarian failure 10
Variation	info
Gene	MCM8
CLNDBN	not provided Premature ovarian failure 10
Reversed	0
HGVS	NC_000020.10:g.5935857C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000148343.1, RCV000162356.4,