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rs774281852

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774281852(C;G)
Make rs774281852(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position45553514
GeneOPA3
is asnp
is mentioned by
dbSNPrs774281852
ebirs774281852
HLIrs774281852
Exacrs774281852
Varsomers774281852
Maprs774281852
PheGenIrs774281852
hapmaprs774281852
1000 genomesrs774281852
hgdprs774281852
ensemblrs774281852
gopubmedrs774281852
geneviewrs774281852
scholarrs774281852
googlers774281852
pharmgkbrs774281852
gwascentralrs774281852
openSNPrs774281852
23andMers774281852
23andMe allrs774281852
SNP Nexus

SNPshotrs774281852
SNPdbers774281852
MSV3drs774281852
GWAS Ctlgrs774281852
Max Magnitude0
ClinVar
Risk rs774281852(G,T;G,T)
Alt rs774281852(G,T;G,T)
Reference rs774281852(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OPA3
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.46056772C>G
CLNSRC
CLNACC RCV000199038.1,