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rs768323248

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768323248(C;T)
Make rs768323248(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95637357
GeneALDH18A1
is asnp
is mentioned by
dbSNPrs768323248
ebirs768323248
HLIrs768323248
Exacrs768323248
Varsomers768323248
Maprs768323248
PheGenIrs768323248
hapmaprs768323248
1000 genomesrs768323248
hgdprs768323248
ensemblrs768323248
gopubmedrs768323248
geneviewrs768323248
scholarrs768323248
googlers768323248
pharmgkbrs768323248
gwascentralrs768323248
openSNPrs768323248
23andMers768323248
23andMe allrs768323248
SNP Nexus

SNPshotrs768323248
SNPdbers768323248
MSV3drs768323248
GWAS Ctlgrs768323248
Max Magnitude0
ClinVar
Risk rs768323248(T;T)
Alt rs768323248(T;T)
Reference rs768323248(C;C)
Significance Pathogenic
Disease Spastic paraplegia 9b
Variation info
Gene ALDH18A1
CLNDBN Spastic paraplegia 9b, autosomal recessive
Reversed 0
HGVS NC_000010.10:g.97397114C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000200953.2,