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rs1005670966

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position12351097
GeneAFG3L2
is asnp
is mentioned by
dbSNPrs1005670966
dbSNP (old)rs1005670966
ClinGenrs1005670966
ebirs1005670966
HLIrs1005670966
Exacrs1005670966
Gnomadrs1005670966
Varsomers1005670966
Maprs1005670966
PheGenIrs1005670966
Biobankrs1005670966
1000 genomesrs1005670966
hgdprs1005670966
ensemblrs1005670966
gopubmedrs1005670966
geneviewrs1005670966
scholarrs1005670966
googlers1005670966
pharmgkbrs1005670966
gwascentralrs1005670966
openSNPrs1005670966
23andMers1005670966
23andMe allrs1005670966
SNP Nexus

SNPshotrs1005670966
SNPdbers1005670966
MSV3drs1005670966
GWAS Ctlgrs1005670966
Max Magnitude0
ClinVar
Risk rs1005670966(A;A)
Alt rs1005670966(A;A)
Reference Rs1005670966(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AFG3L2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.12351096G>A
CLNSRC
CLNACC RCV000489336.1,