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rs878853397

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853397(-;-)
Make rs878853397(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position94043428
GeneABCA4
is asnp
is mentioned by
dbSNPrs878853397
ebirs878853397
HLIrs878853397
Exacrs878853397
Varsomers878853397
Maprs878853397
PheGenIrs878853397
hapmaprs878853397
1000 genomesrs878853397
hgdprs878853397
ensemblrs878853397
gopubmedrs878853397
geneviewrs878853397
scholarrs878853397
googlers878853397
pharmgkbrs878853397
gwascentralrs878853397
openSNPrs878853397
23andMers878853397
23andMe allrs878853397
SNP Nexus

SNPshotrs878853397
SNPdbers878853397
MSV3drs878853397
GWAS Ctlgrs878853397
Max Magnitude0
ClinVar
Risk rs878853397(;)
Alt rs878853397(;)
Reference rs878853397(A;A)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene ABCA4
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000001.10:g.94508984delT
CLNSRC
CLNACC RCV000225375.1,