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rs863224127

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224127(A;A)
Make rs863224127(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position193631616
GeneOPA1
is asnp
is mentioned by
dbSNPrs863224127
dbSNP (classic)rs863224127
ClinGenrs863224127
ebirs863224127
HLIrs863224127
Exacrs863224127
Gnomadrs863224127
Varsomers863224127
LitVarrs863224127
Maprs863224127
PheGenIrs863224127
Biobankrs863224127
1000 genomesrs863224127
hgdprs863224127
ensemblrs863224127
geneviewrs863224127
scholarrs863224127
googlers863224127
pharmgkbrs863224127
gwascentralrs863224127
openSNPrs863224127
23andMers863224127
SNPshotrs863224127
SNPdbers863224127
MSV3drs863224127
GWAS Ctlgrs863224127
Max Magnitude0
ClinVar
Risk rs863224127(A;A)
Alt rs863224127(A;A)
Reference Rs863224127(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OPA1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.193349405C>A
CLNSRC
CLNACC RCV000199764.1,