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rs752669339

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752669339(C;G)
Make rs752669339(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95610260
GeneALDH18A1
is asnp
is mentioned by
dbSNPrs752669339
ebirs752669339
HLIrs752669339
Exacrs752669339
Varsomers752669339
Maprs752669339
PheGenIrs752669339
hapmaprs752669339
1000 genomesrs752669339
hgdprs752669339
ensemblrs752669339
gopubmedrs752669339
geneviewrs752669339
scholarrs752669339
googlers752669339
pharmgkbrs752669339
gwascentralrs752669339
openSNPrs752669339
23andMers752669339
23andMe allrs752669339
SNP Nexus

SNPshotrs752669339
SNPdbers752669339
MSV3drs752669339
GWAS Ctlgrs752669339
Max Magnitude0
ClinVar
Risk rs752669339(G;G)
Alt rs752669339(G;G)
Reference rs752669339(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.97370017C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000200955.2,