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rs766264810

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766264810(C;T)
Make rs766264810(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95611372
GeneALDH18A1
is asnp
is mentioned by
dbSNPrs766264810
ebirs766264810
HLIrs766264810
Exacrs766264810
Varsomers766264810
Maprs766264810
PheGenIrs766264810
hapmaprs766264810
1000 genomesrs766264810
hgdprs766264810
ensemblrs766264810
gopubmedrs766264810
geneviewrs766264810
scholarrs766264810
googlers766264810
pharmgkbrs766264810
gwascentralrs766264810
openSNPrs766264810
23andMers766264810
23andMe allrs766264810
SNP Nexus

SNPshotrs766264810
SNPdbers766264810
MSV3drs766264810
GWAS Ctlgrs766264810
Max Magnitude0
ClinVar
Risk rs766264810(T;T)
Alt rs766264810(T;T)
Reference rs766264810(C;C)
Significance Pathogenic
Disease Spastic paraplegia 9
Variation info
Gene ALDH18A1
CLNDBN Spastic paraplegia 9
Reversed 0
HGVS NC_000010.10:g.97371129C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000200958.2,