Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224258

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224258(G;T)
Make rs863224258(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position96231067
GeneUQCRB
is asnp
is mentioned by
dbSNPrs863224258
ebirs863224258
HLIrs863224258
Exacrs863224258
Varsomers863224258
Maprs863224258
PheGenIrs863224258
hapmaprs863224258
1000 genomesrs863224258
hgdprs863224258
ensemblrs863224258
gopubmedrs863224258
geneviewrs863224258
scholarrs863224258
googlers863224258
pharmgkbrs863224258
gwascentralrs863224258
openSNPrs863224258
23andMers863224258
23andMe allrs863224258
SNP Nexus

SNPshotrs863224258
SNPdbers863224258
MSV3drs863224258
GWAS Ctlgrs863224258
Max Magnitude0
ClinVar
Risk rs863224258(T;T)
Alt rs863224258(T;T)
Reference rs863224258(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene UQCRB
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.97243295C>A
CLNSRC
CLNACC RCV000196431.1,