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rs1064793795

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome16
Position70483871
GeneCOG4
is asnp
is mentioned by
dbSNPrs1064793795
dbSNP (old)rs1064793795
ClinGenrs1064793795
ebirs1064793795
HLIrs1064793795
Exacrs1064793795
Gnomadrs1064793795
Varsomers1064793795
LitVarrs1064793795
Maprs1064793795
PheGenIrs1064793795
Biobankrs1064793795
1000 genomesrs1064793795
hgdprs1064793795
ensemblrs1064793795
gopubmedrs1064793795
geneviewrs1064793795
scholarrs1064793795
googlers1064793795
pharmgkbrs1064793795
gwascentralrs1064793795
openSNPrs1064793795
23andMers1064793795
23andMe allrs1064793795
SNPshotrs1064793795
SNPdbers1064793795
MSV3drs1064793795
GWAS Ctlgrs1064793795
Max Magnitude0
ClinVar
Risk rs1064793795(-;-)
Alt rs1064793795(-;-)
Reference Rs1064793795(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COG4
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.70517774delT
CLNSRC
CLNACC RCV000479342.1,