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rs864321669

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864321669(C;C)
Make rs864321669(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95633040
GeneALDH18A1
is asnp
is mentioned by
dbSNPrs864321669
ebirs864321669
HLIrs864321669
Exacrs864321669
Varsomers864321669
Maprs864321669
PheGenIrs864321669
hapmaprs864321669
1000 genomesrs864321669
hgdprs864321669
ensemblrs864321669
gopubmedrs864321669
geneviewrs864321669
scholarrs864321669
googlers864321669
pharmgkbrs864321669
gwascentralrs864321669
openSNPrs864321669
23andMers864321669
23andMe allrs864321669
SNP Nexus

SNPshotrs864321669
SNPdbers864321669
MSV3drs864321669
GWAS Ctlgrs864321669
Max Magnitude0
ClinVar
Risk rs864321669(C;C)
Alt rs864321669(C;C)
Reference rs864321669(G;G)
Significance Pathogenic
Disease Spastic paraplegia 9
Variation info
Gene ALDH18A1
CLNDBN Spastic paraplegia 9
Reversed 1
HGVS NC_000010.10:g.97392797C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000200956.2,