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

rs151344513

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151344513(C;T)
Make rs151344513(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position12340220
GeneAFG3L2
is asnp
is mentioned by
dbSNPrs151344513
ebirs151344513
HLIrs151344513
Exacrs151344513
Varsomers151344513
Maprs151344513
PheGenIrs151344513
hapmaprs151344513
1000 genomesrs151344513
hgdprs151344513
ensemblrs151344513
gopubmedrs151344513
geneviewrs151344513
scholarrs151344513
googlers151344513
pharmgkbrs151344513
gwascentralrs151344513
openSNPrs151344513
23andMers151344513
23andMe allrs151344513
SNP Nexus

SNPshotrs151344513
SNPdbers151344513
MSV3drs151344513
GWAS Ctlgrs151344513
Max Magnitude0
ClinVar
Risk rs151344513(T;T)
Alt rs151344513(T;T)
Reference rs151344513(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia 28
Variation info
Gene AFG3L2
CLNDBN Spinocerebellar ataxia 28
Reversed 1
HGVS NC_000018.9:g.12340219G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000031941.2,