rs138761187

Orientation

plus

Stabilized

plus

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

Make rs138761187(A;A)

Make rs138761187(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

5985921

Gene

MCM8

is a	snp
is	mentioned by
dbSNP	rs138761187
dbSNP (classic)	rs138761187
ClinGen	rs138761187
ebi	rs138761187
HLI	rs138761187
Exac	rs138761187
Gnomad	rs138761187
Varsome	rs138761187
LitVar	rs138761187
Map	rs138761187
PheGenI	rs138761187
Biobank	rs138761187
1000 genomes	rs138761187
hgdp	rs138761187
ensembl	rs138761187
geneview	rs138761187
scholar	rs138761187
google	rs138761187
pharmgkb	rs138761187
gwascentral	rs138761187
openSNP	rs138761187
23andMe	rs138761187
SNPshot	rs138761187
SNPdbe	rs138761187
MSV3d	rs138761187
GWAS Ctlg	rs138761187

Max Magnitude

0

ClinVar
Risk	rs138761187(A;A)
Alt	rs138761187(A;A)
Reference	Rs138761187(G;G)
Significance	Pathogenic
Disease	Premature ovarian failure 10
Variation	info
Gene	MCM8
CLNDBN	Premature ovarian failure 10
Reversed	0
HGVS	NC_000020.10:g.5966567G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000190838.4,