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rs863224132

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224132(A;G)
Make rs863224132(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position193638042
GeneOPA1
is asnp
is mentioned by
dbSNPrs863224132
ebirs863224132
HLIrs863224132
Exacrs863224132
Varsomers863224132
Maprs863224132
PheGenIrs863224132
hapmaprs863224132
1000 genomesrs863224132
hgdprs863224132
ensemblrs863224132
gopubmedrs863224132
geneviewrs863224132
scholarrs863224132
googlers863224132
pharmgkbrs863224132
gwascentralrs863224132
openSNPrs863224132
23andMers863224132
23andMe allrs863224132
SNP Nexus

SNPshotrs863224132
SNPdbers863224132
MSV3drs863224132
GWAS Ctlgrs863224132
Max Magnitude0
ClinVar
Risk rs863224132(G;G)
Alt rs863224132(G;G)
Reference rs863224132(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OPA1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.193355831A>G
CLNSRC
CLNACC RCV000198713.1,