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rs1057518024

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518024(A;A)
Make rs1057518024(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position12358732
GeneAFG3L2
is asnp
is mentioned by
dbSNPrs1057518024
dbSNP (old)rs1057518024
ClinGenrs1057518024
ebirs1057518024
HLIrs1057518024
Exacrs1057518024
Gnomadrs1057518024
Varsomers1057518024
Maprs1057518024
PheGenIrs1057518024
Biobankrs1057518024
1000 genomesrs1057518024
hgdprs1057518024
ensemblrs1057518024
gopubmedrs1057518024
geneviewrs1057518024
scholarrs1057518024
googlers1057518024
pharmgkbrs1057518024
gwascentralrs1057518024
openSNPrs1057518024
23andMers1057518024
23andMe allrs1057518024
SNPshotrs1057518024
SNPdbers1057518024
MSV3drs1057518024
GWAS Ctlgrs1057518024
Max Magnitude0
ClinVar
Risk rs1057518024(A;A)
Alt rs1057518024(A;A)
Reference Rs1057518024(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AFG3L2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.12358731C>T
CLNSRC
CLNACC RCV000413869.1,