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rs869320690

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869320690(C;C)
Make rs869320690(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position95613755
GeneALDH18A1
is asnp
is mentioned by
dbSNPrs869320690
ebirs869320690
HLIrs869320690
Exacrs869320690
Varsomers869320690
Maprs869320690
PheGenIrs869320690
hapmaprs869320690
1000 genomesrs869320690
hgdprs869320690
ensemblrs869320690
gopubmedrs869320690
geneviewrs869320690
scholarrs869320690
googlers869320690
pharmgkbrs869320690
gwascentralrs869320690
openSNPrs869320690
23andMers869320690
23andMe allrs869320690
SNP Nexus

SNPshotrs869320690
SNPdbers869320690
MSV3drs869320690
GWAS Ctlgrs869320690
Max Magnitude0
ClinVar
Risk rs869320690(C;C)
Alt rs869320690(C;C)
Reference rs869320690(T;T)
Significance Pathogenic
Disease Spastic paraplegia 9b
Variation info
Gene ALDH18A1
CLNDBN Spastic paraplegia 9b, autosomal recessive
Reversed 1
HGVS NC_000010.10:g.97373512A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000200952.1,