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rs863224135

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224135(C;C)
Make rs863224135(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position193643440
GeneOPA1
is asnp
is mentioned by
dbSNPrs863224135
ebirs863224135
HLIrs863224135
Exacrs863224135
Varsomers863224135
Maprs863224135
PheGenIrs863224135
hapmaprs863224135
1000 genomesrs863224135
hgdprs863224135
ensemblrs863224135
gopubmedrs863224135
geneviewrs863224135
scholarrs863224135
googlers863224135
pharmgkbrs863224135
gwascentralrs863224135
openSNPrs863224135
23andMers863224135
23andMe allrs863224135
SNP Nexus

SNPshotrs863224135
SNPdbers863224135
MSV3drs863224135
GWAS Ctlgrs863224135
Max Magnitude0
ClinVar
Risk rs863224135(C;C)
Alt rs863224135(C;C)
Reference rs863224135(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OPA1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.193361229T>C
CLNSRC
CLNACC RCV000198337.1,