Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064796804

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome18
Position12340205
GeneAFG3L2, LOC107985154
is asnp
is mentioned by
dbSNPrs1064796804
dbSNP (classic)rs1064796804
ClinGenrs1064796804
ebirs1064796804
HLIrs1064796804
Exacrs1064796804
Gnomadrs1064796804
Varsomers1064796804
LitVarrs1064796804
Maprs1064796804
PheGenIrs1064796804
Biobankrs1064796804
1000 genomesrs1064796804
hgdprs1064796804
ensemblrs1064796804
geneviewrs1064796804
scholarrs1064796804
googlers1064796804
pharmgkbrs1064796804
gwascentralrs1064796804
openSNPrs1064796804
23andMers1064796804
SNPshotrs1064796804
SNPdbers1064796804
MSV3drs1064796804
GWAS Ctlgrs1064796804
Max Magnitude0
ClinVar
Risk rs1064796804(T;T)
Alt rs1064796804(T;T)
Reference Rs1064796804(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AFG3L2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.12340204G>A
CLNSRC
CLNACC RCV000482649.1,