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

rs878853400

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853400(-;-)
Make rs878853400(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position15984327
GenePROM1
is asnp
is mentioned by
dbSNPrs878853400
ebirs878853400
HLIrs878853400
Exacrs878853400
Varsomers878853400
Maprs878853400
PheGenIrs878853400
hapmaprs878853400
1000 genomesrs878853400
hgdprs878853400
ensemblrs878853400
gopubmedrs878853400
geneviewrs878853400
scholarrs878853400
googlers878853400
pharmgkbrs878853400
gwascentralrs878853400
openSNPrs878853400
23andMers878853400
23andMe allrs878853400
SNP Nexus

SNPshotrs878853400
SNPdbers878853400
MSV3drs878853400
GWAS Ctlgrs878853400
Max Magnitude0
ClinVar
Risk rs878853400(;)
Alt rs878853400(;)
Reference rs878853400(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene PROM1
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000004.11:g.15985950delG
CLNSRC
CLNACC RCV000225433.1,