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rs878853396

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853396(C;T)
Make rs878853396(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position94062641
GeneABCA4
is asnp
is mentioned by
dbSNPrs878853396
ebirs878853396
HLIrs878853396
Exacrs878853396
Varsomers878853396
Maprs878853396
PheGenIrs878853396
hapmaprs878853396
1000 genomesrs878853396
hgdprs878853396
ensemblrs878853396
gopubmedrs878853396
geneviewrs878853396
scholarrs878853396
googlers878853396
pharmgkbrs878853396
gwascentralrs878853396
openSNPrs878853396
23andMers878853396
23andMe allrs878853396
SNP Nexus

SNPshotrs878853396
SNPdbers878853396
MSV3drs878853396
GWAS Ctlgrs878853396
Max Magnitude0
ClinVar
Risk rs878853396(T;T)
Alt rs878853396(T;T)
Reference rs878853396(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene ABCA4
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000001.10:g.94528197G>A
CLNSRC
CLNACC RCV000225610.1,