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rs1064794917

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome22
Position31754984
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs1064794917
dbSNP (classic)rs1064794917
ClinGenrs1064794917
ebirs1064794917
HLIrs1064794917
Exacrs1064794917
Gnomadrs1064794917
Varsomers1064794917
LitVarrs1064794917
Maprs1064794917
PheGenIrs1064794917
Biobankrs1064794917
1000 genomesrs1064794917
hgdprs1064794917
ensemblrs1064794917
geneviewrs1064794917
scholarrs1064794917
googlers1064794917
pharmgkbrs1064794917
gwascentralrs1064794917
openSNPrs1064794917
23andMers1064794917
23andMe allrs1064794917
SNPshotrs1064794917
SNPdbers1064794917
MSV3drs1064794917
GWAS Ctlgrs1064794917
Max Magnitude0
ClinVar
Risk rs1064794917(C;C)
Alt rs1064794917(C;C)
Reference Rs1064794917(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DEPDC5
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.32150970G>C
CLNSRC
CLNACC RCV000480307.1,