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rs863224878

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224878(C;T)
Make rs863224878(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position197487161
GeneHSPD1, SNORA105B
is asnp
is mentioned by
dbSNPrs863224878
ebirs863224878
HLIrs863224878
Exacrs863224878
Varsomers863224878
Maprs863224878
PheGenIrs863224878
hapmaprs863224878
1000 genomesrs863224878
hgdprs863224878
ensemblrs863224878
gopubmedrs863224878
geneviewrs863224878
scholarrs863224878
googlers863224878
pharmgkbrs863224878
gwascentralrs863224878
openSNPrs863224878
23andMers863224878
23andMe allrs863224878
SNP Nexus

SNPshotrs863224878
SNPdbers863224878
MSV3drs863224878
GWAS Ctlgrs863224878
Max Magnitude0
ClinVar
Risk rs863224878(T;T)
Alt rs863224878(T;T)
Reference rs863224878(C;C)
Significance Probable-Pathogenic
Disease Spastic paraplegia 13
Variation info
Gene HSPD1 SNORA105B
CLNDBN Spastic paraplegia 13
Reversed 1
HGVS NC_000002.11:g.198351885G>A
CLNSRC
CLNACC RCV000200544.1,