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rs863224870

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224870(C;T)
Make rs863224870(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position74726321
GeneFA2H
is asnp
is mentioned by
dbSNPrs863224870
ebirs863224870
HLIrs863224870
Exacrs863224870
Varsomers863224870
Maprs863224870
PheGenIrs863224870
hapmaprs863224870
1000 genomesrs863224870
hgdprs863224870
ensemblrs863224870
gopubmedrs863224870
geneviewrs863224870
scholarrs863224870
googlers863224870
pharmgkbrs863224870
gwascentralrs863224870
openSNPrs863224870
23andMers863224870
23andMe allrs863224870
SNP Nexus

SNPshotrs863224870
SNPdbers863224870
MSV3drs863224870
GWAS Ctlgrs863224870
Max Magnitude0
ClinVar
Risk rs863224870(T;T)
Alt rs863224870(T;T)
Reference rs863224870(C;C)
Significance Probable-Pathogenic
Disease Spastic paraplegia 35
Variation info
Gene FA2H
CLNDBN Spastic paraplegia 35
Reversed 1
HGVS NC_000016.9:g.74760219G>A
CLNSRC
CLNACC RCV000199368.1,