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rs863224257

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224257(A;T)
Make rs863224257(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position96233191
GeneUQCRB
is asnp
is mentioned by
dbSNPrs863224257
ebirs863224257
HLIrs863224257
Exacrs863224257
Varsomers863224257
Maprs863224257
PheGenIrs863224257
hapmaprs863224257
1000 genomesrs863224257
hgdprs863224257
ensemblrs863224257
gopubmedrs863224257
geneviewrs863224257
scholarrs863224257
googlers863224257
pharmgkbrs863224257
gwascentralrs863224257
openSNPrs863224257
23andMers863224257
23andMe allrs863224257
SNP Nexus

SNPshotrs863224257
SNPdbers863224257
MSV3drs863224257
GWAS Ctlgrs863224257
Max Magnitude0
ClinVar
Risk rs863224257(T;T)
Alt rs863224257(T;T)
Reference rs863224257(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene UQCRB
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.97245419T>A
CLNSRC
CLNACC RCV000200023.1,