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rs1064795606

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome18
Position45900994
GeneEPG5
is asnp
is mentioned by
dbSNPrs1064795606
dbSNP (old)rs1064795606
ClinGenrs1064795606
ebirs1064795606
HLIrs1064795606
Exacrs1064795606
Gnomadrs1064795606
Varsomers1064795606
Maprs1064795606
PheGenIrs1064795606
Biobankrs1064795606
1000 genomesrs1064795606
hgdprs1064795606
ensemblrs1064795606
gopubmedrs1064795606
geneviewrs1064795606
scholarrs1064795606
googlers1064795606
pharmgkbrs1064795606
gwascentralrs1064795606
openSNPrs1064795606
23andMers1064795606
23andMe allrs1064795606
SNPshotrs1064795606
SNPdbers1064795606
MSV3drs1064795606
GWAS Ctlgrs1064795606
Max Magnitude0
ClinVar
Risk rs1064795606(C;C)
Alt rs1064795606(C;C)
Reference Rs1064795606(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EPG5
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.43480959A>G
CLNSRC
CLNACC RCV000481769.1,