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rs1064795689

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Chromosome1
Position154588141
GeneADAR
is asnp
is mentioned by
dbSNPrs1064795689
dbSNP (old)rs1064795689
ClinGenrs1064795689
ebirs1064795689
HLIrs1064795689
Exacrs1064795689
Gnomadrs1064795689
Varsomers1064795689
Maprs1064795689
PheGenIrs1064795689
Biobankrs1064795689
1000 genomesrs1064795689
hgdprs1064795689
ensemblrs1064795689
gopubmedrs1064795689
geneviewrs1064795689
scholarrs1064795689
googlers1064795689
pharmgkbrs1064795689
gwascentralrs1064795689
openSNPrs1064795689
23andMers1064795689
23andMe allrs1064795689
SNPshotrs1064795689
SNPdbers1064795689
MSV3drs1064795689
GWAS Ctlgrs1064795689
Max Magnitude0
ClinVar
Risk rs1064795689(TT;TT)
Alt rs1064795689(TT;TT)
Reference Rs1064795689(GC;GC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ADAR
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.154560617_154560618delGCinsAA
CLNSRC
CLNACC RCV000480726.1,