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rs878853390

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853390(-;-)
Make rs878853390(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position21324862
GeneRPGRIP1
is asnp
is mentioned by
dbSNPrs878853390
ebirs878853390
HLIrs878853390
Exacrs878853390
Varsomers878853390
Maprs878853390
PheGenIrs878853390
hapmaprs878853390
1000 genomesrs878853390
hgdprs878853390
ensemblrs878853390
gopubmedrs878853390
geneviewrs878853390
scholarrs878853390
googlers878853390
pharmgkbrs878853390
gwascentralrs878853390
openSNPrs878853390
23andMers878853390
23andMe allrs878853390
SNP Nexus

SNPshotrs878853390
SNPdbers878853390
MSV3drs878853390
GWAS Ctlgrs878853390
Max Magnitude0
ClinVar
Risk rs878853390(;)
Alt rs878853390(;)
Reference rs878853390(T;T)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene RPGRIP1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000014.8:g.21793021delT
CLNSRC
CLNACC RCV000225615.1,