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rs1057518234

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTGA;TTGA) 0 common in clinvar
Make rs1057518234(-;-)
Make rs1057518234(-;TTGA)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position5954632
GeneMCM8
is asnp
is mentioned by
dbSNPrs1057518234
dbSNP (old)rs1057518234
ClinGenrs1057518234
ebirs1057518234
HLIrs1057518234
Exacrs1057518234
Gnomadrs1057518234
Varsomers1057518234
Maprs1057518234
PheGenIrs1057518234
Biobankrs1057518234
1000 genomesrs1057518234
hgdprs1057518234
ensemblrs1057518234
gopubmedrs1057518234
geneviewrs1057518234
scholarrs1057518234
googlers1057518234
pharmgkbrs1057518234
gwascentralrs1057518234
openSNPrs1057518234
23andMers1057518234
23andMe allrs1057518234
SNPshotrs1057518234
SNPdbers1057518234
MSV3drs1057518234
GWAS Ctlgrs1057518234
Max Magnitude0
ClinVar
Risk rs1057518234(-;-)
Alt rs1057518234(-;-)
Reference Rs1057518234(TTGA;TTGA)
Significance Pathogenic
Disease not provided
Variation info
Gene MCM8
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.5935278_5935281delTTGA
CLNSRC
CLNACC RCV000414339.1,