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rs878853389

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853389(-;-)
Make rs878853389(-;A)
Make rs878853389(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position21326071
GeneRPGRIP1
is asnp
is mentioned by
dbSNPrs878853389
ebirs878853389
HLIrs878853389
Exacrs878853389
Varsomers878853389
Maprs878853389
PheGenIrs878853389
hapmaprs878853389
1000 genomesrs878853389
hgdprs878853389
ensemblrs878853389
gopubmedrs878853389
geneviewrs878853389
scholarrs878853389
googlers878853389
pharmgkbrs878853389
gwascentralrs878853389
openSNPrs878853389
23andMers878853389
23andMe allrs878853389
SNP Nexus

SNPshotrs878853389
SNPdbers878853389
MSV3drs878853389
GWAS Ctlgrs878853389
Max Magnitude0
ClinVar
Risk rs878853389(A;A)
Alt rs878853389(A;A)
Reference rs878853389(;)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene RPGRIP1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000014.8:g.21794230_21794231insA
CLNSRC
CLNACC RCV000225501.1,