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

rs864321670

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864321670(A;A)
Make rs864321670(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95633012
GeneALDH18A1
is asnp
is mentioned by
dbSNPrs864321670
ebirs864321670
HLIrs864321670
Exacrs864321670
Varsomers864321670
Maprs864321670
PheGenIrs864321670
hapmaprs864321670
1000 genomesrs864321670
hgdprs864321670
ensemblrs864321670
gopubmedrs864321670
geneviewrs864321670
scholarrs864321670
googlers864321670
pharmgkbrs864321670
gwascentralrs864321670
openSNPrs864321670
23andMers864321670
23andMe allrs864321670
SNP Nexus

SNPshotrs864321670
SNPdbers864321670
MSV3drs864321670
GWAS Ctlgrs864321670
Max Magnitude0
ClinVar
Risk rs864321670(A;A)
Alt rs864321670(A;A)
Reference rs864321670(G;G)
Significance Pathogenic
Disease Spastic paraplegia 9
Variation info
Gene ALDH18A1
CLNDBN Spastic paraplegia 9
Reversed 1
HGVS NC_000010.10:g.97392769C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000200959.2,