Have questions? Visit https://www.reddit.com/r/SNPedia

rs869320753

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869320753(-;-)
Make rs869320753(-;TA)
Make rs869320753(TA;TA)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position5977950
GeneMCM8
is asnp
is mentioned by
dbSNPrs869320753
ebirs869320753
HLIrs869320753
Exacrs869320753
Varsomers869320753
Maprs869320753
PheGenIrs869320753
hapmaprs869320753
1000 genomesrs869320753
hgdprs869320753
ensemblrs869320753
gopubmedrs869320753
geneviewrs869320753
scholarrs869320753
googlers869320753
pharmgkbrs869320753
gwascentralrs869320753
openSNPrs869320753
23andMers869320753
23andMe allrs869320753
SNP Nexus

SNPshotrs869320753
SNPdbers869320753
MSV3drs869320753
GWAS Ctlgrs869320753
Max Magnitude0
ClinVar
Risk rs869320753(TA;TA)
Alt rs869320753(TA;TA)
Reference rs869320753(;)
Significance Pathogenic
Disease Premature ovarian failure 10
Variation info
Gene MCM8
CLNDBN Premature ovarian failure 10
Reversed 0
HGVS NC_000020.10:g.5958596_5958597insTA
CLNSRC OMIM Allelic Variant
CLNACC RCV000190839.3,