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rs1064795281

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome18
Position12356705
GeneAFG3L2
is asnp
is mentioned by
dbSNPrs1064795281
dbSNP (old)rs1064795281
ClinGenrs1064795281
ebirs1064795281
HLIrs1064795281
Exacrs1064795281
Gnomadrs1064795281
Varsomers1064795281
Maprs1064795281
PheGenIrs1064795281
Biobankrs1064795281
1000 genomesrs1064795281
hgdprs1064795281
ensemblrs1064795281
gopubmedrs1064795281
geneviewrs1064795281
scholarrs1064795281
googlers1064795281
pharmgkbrs1064795281
gwascentralrs1064795281
openSNPrs1064795281
23andMers1064795281
23andMe allrs1064795281
SNPshotrs1064795281
SNPdbers1064795281
MSV3drs1064795281
GWAS Ctlgrs1064795281
Max Magnitude0
ClinVar
Risk rs1064795281(A;A)
Alt rs1064795281(A;A)
Reference Rs1064795281(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AFG3L2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.12356704C>T
CLNSRC
CLNACC RCV000486261.1,