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rs1064794869

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position219418592
GeneDES
is asnp
is mentioned by
dbSNPrs1064794869
dbSNP (old)rs1064794869
ClinGenrs1064794869
ebirs1064794869
HLIrs1064794869
Exacrs1064794869
Gnomadrs1064794869
Varsomers1064794869
Maprs1064794869
PheGenIrs1064794869
Biobankrs1064794869
1000 genomesrs1064794869
hgdprs1064794869
ensemblrs1064794869
gopubmedrs1064794869
geneviewrs1064794869
scholarrs1064794869
googlers1064794869
pharmgkbrs1064794869
gwascentralrs1064794869
openSNPrs1064794869
23andMers1064794869
23andMe allrs1064794869
SNPshotrs1064794869
SNPdbers1064794869
MSV3drs1064794869
GWAS Ctlgrs1064794869
Max Magnitude0
ClinVar
Risk rs1064794869(A;A)
Alt rs1064794869(A;A)
Reference Rs1064794869(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DES
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220283314G>A
CLNSRC
CLNACC RCV000478404.1,