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rs863224220

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224220(A;A)
Make rs863224220(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89548093
GeneSPG7
is asnp
is mentioned by
dbSNPrs863224220
ebirs863224220
HLIrs863224220
Exacrs863224220
Varsomers863224220
Maprs863224220
PheGenIrs863224220
hapmaprs863224220
1000 genomesrs863224220
hgdprs863224220
ensemblrs863224220
gopubmedrs863224220
geneviewrs863224220
scholarrs863224220
googlers863224220
pharmgkbrs863224220
gwascentralrs863224220
openSNPrs863224220
23andMers863224220
23andMe allrs863224220
SNP Nexus

SNPshotrs863224220
SNPdbers863224220
MSV3drs863224220
GWAS Ctlgrs863224220
Max Magnitude0
ClinVar
Risk rs863224220(A;A)
Alt rs863224220(A;A)
Reference rs863224220(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RPL13 SPG7
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89614501C>A
CLNSRC
CLNACC RCV000197084.2,