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rs878853381

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853381(-;-)
Make rs878853381(-;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position46853880
GeneRP2
is asnp
is mentioned by
dbSNPrs878853381
ebirs878853381
HLIrs878853381
Exacrs878853381
Varsomers878853381
Maprs878853381
PheGenIrs878853381
hapmaprs878853381
1000 genomesrs878853381
hgdprs878853381
ensemblrs878853381
gopubmedrs878853381
geneviewrs878853381
scholarrs878853381
googlers878853381
pharmgkbrs878853381
gwascentralrs878853381
openSNPrs878853381
23andMers878853381
23andMe allrs878853381
SNP Nexus

SNPshotrs878853381
SNPdbers878853381
MSV3drs878853381
GWAS Ctlgrs878853381
Max Magnitude0
ClinVar
Risk rs878853381(;)
Alt rs878853381(;)
Reference rs878853381(T;T)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene RP2
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000023.10:g.46713315delT
CLNSRC
CLNACC RCV000225675.1,