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rs863224141

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs863224141(ATA;ATA)
Make rs863224141(ATA;CTT)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position193617260
GeneOPA1
is asnp
is mentioned by
dbSNPrs863224141
dbSNP (old)rs863224141
ClinGenrs863224141
ebirs863224141
HLIrs863224141
Exacrs863224141
Gnomadrs863224141
Varsomers863224141
Maprs863224141
PheGenIrs863224141
Biobankrs863224141
1000 genomesrs863224141
hgdprs863224141
ensemblrs863224141
gopubmedrs863224141
geneviewrs863224141
scholarrs863224141
googlers863224141
pharmgkbrs863224141
gwascentralrs863224141
openSNPrs863224141
23andMers863224141
23andMe allrs863224141
SNP Nexus

SNPshotrs863224141
SNPdbers863224141
MSV3drs863224141
GWAS Ctlgrs863224141
Max Magnitude0
ClinVar
Risk rs863224141(ATA;ATA)
Alt rs863224141(ATA;ATA)
Reference Rs863224141(CTT;CTT)
Significance Pathogenic
Disease not provided
Variation info
Gene OPA1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.193335049_193335051delCTTinsATA
CLNSRC
CLNACC RCV000199579.1,