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rs863224223

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224223(-;-)
Make rs863224223(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89556894
GeneSPG7
is asnp
is mentioned by
dbSNPrs863224223
dbSNP (classic)rs863224223
ClinGenrs863224223
ebirs863224223
HLIrs863224223
Exacrs863224223
Gnomadrs863224223
Varsomers863224223
LitVarrs863224223
Maprs863224223
PheGenIrs863224223
Biobankrs863224223
1000 genomesrs863224223
hgdprs863224223
ensemblrs863224223
geneviewrs863224223
scholarrs863224223
googlers863224223
pharmgkbrs863224223
gwascentralrs863224223
openSNPrs863224223
23andMers863224223
SNPshotrs863224223
SNPdbers863224223
MSV3drs863224223
GWAS Ctlgrs863224223
Max Magnitude0
ClinVar
Risk rs863224223(-;-)
Alt rs863224223(-;-)
Reference Rs863224223(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL13 SPG7
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89623302delA
CLNSRC
CLNACC RCV000195477.1,