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rs151344520

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151344520(A;A)
Make rs151344520(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position12337445
GeneAFG3L2
is asnp
is mentioned by
dbSNPrs151344520
ebirs151344520
HLIrs151344520
Exacrs151344520
Varsomers151344520
Maprs151344520
PheGenIrs151344520
hapmaprs151344520
1000 genomesrs151344520
hgdprs151344520
ensemblrs151344520
gopubmedrs151344520
geneviewrs151344520
scholarrs151344520
googlers151344520
pharmgkbrs151344520
gwascentralrs151344520
openSNPrs151344520
23andMers151344520
23andMe allrs151344520
SNP Nexus

SNPshotrs151344520
SNPdbers151344520
MSV3drs151344520
GWAS Ctlgrs151344520
Max Magnitude0
ClinVar
Risk rs151344520(A;A)
Alt rs151344520(A;A)
Reference rs151344520(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia 28
Variation info
Gene AFG3L2
CLNDBN Spinocerebellar ataxia 28
Reversed 1
HGVS NC_000018.9:g.12337444C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005804.2,