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rs368488165

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368488165(C;T)
Make rs368488165(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position193614901
GeneOPA1
is asnp
is mentioned by
dbSNPrs368488165
ebirs368488165
HLIrs368488165
Exacrs368488165
Varsomers368488165
Maprs368488165
PheGenIrs368488165
hapmaprs368488165
1000 genomesrs368488165
hgdprs368488165
ensemblrs368488165
gopubmedrs368488165
geneviewrs368488165
scholarrs368488165
googlers368488165
pharmgkbrs368488165
gwascentralrs368488165
openSNPrs368488165
23andMers368488165
23andMe allrs368488165
SNP Nexus

SNPshotrs368488165
SNPdbers368488165
MSV3drs368488165
GWAS Ctlgrs368488165
Max Magnitude0
ClinVar
Risk rs368488165(T;T)
Alt rs368488165(T;T)
Reference rs368488165(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OPA1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.193332690C>T
CLNSRC
CLNACC RCV000198796.1,