Have questions? Visit https://www.reddit.com/r/SNPedia

rs878855330

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855330(C;C)
Make rs878855330(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position109241226
GeneACACB
is asnp
is mentioned by
dbSNPrs878855330
ebirs878855330
HLIrs878855330
Exacrs878855330
Varsomers878855330
Maprs878855330
PheGenIrs878855330
hapmaprs878855330
1000 genomesrs878855330
hgdprs878855330
ensemblrs878855330
gopubmedrs878855330
geneviewrs878855330
scholarrs878855330
googlers878855330
pharmgkbrs878855330
gwascentralrs878855330
openSNPrs878855330
23andMers878855330
23andMe allrs878855330
SNP Nexus

SNPshotrs878855330
SNPdbers878855330
MSV3drs878855330
GWAS Ctlgrs878855330
Max Magnitude0
ClinVar
Risk rs878855330(C;C)
Alt rs878855330(C;C)
Reference rs878855330(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene ACACB
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000012.11:g.109679031G>C
CLNSRC
CLNACC RCV000234829.1,