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rs863224134

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224134(C;C)
Make rs863224134(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position193648872
GeneLOC102724808, OPA1
is asnp
is mentioned by
dbSNPrs863224134
ebirs863224134
HLIrs863224134
Exacrs863224134
Varsomers863224134
Maprs863224134
PheGenIrs863224134
hapmaprs863224134
1000 genomesrs863224134
hgdprs863224134
ensemblrs863224134
gopubmedrs863224134
geneviewrs863224134
scholarrs863224134
googlers863224134
pharmgkbrs863224134
gwascentralrs863224134
openSNPrs863224134
23andMers863224134
23andMe allrs863224134
SNP Nexus

SNPshotrs863224134
SNPdbers863224134
MSV3drs863224134
GWAS Ctlgrs863224134
Max Magnitude0
ClinVar
Risk rs863224134(C;C)
Alt rs863224134(C;C)
Reference rs863224134(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OPA1 LOC101929213
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.193366661G>C
CLNSRC
CLNACC RCV000197138.2,