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rs869312184

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312184(-;-)
Make rs869312184(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position94048898
GeneABCA4
is asnp
is mentioned by
dbSNPrs869312184
ebirs869312184
HLIrs869312184
Exacrs869312184
Varsomers869312184
Maprs869312184
PheGenIrs869312184
hapmaprs869312184
1000 genomesrs869312184
hgdprs869312184
ensemblrs869312184
gopubmedrs869312184
geneviewrs869312184
scholarrs869312184
googlers869312184
pharmgkbrs869312184
gwascentralrs869312184
openSNPrs869312184
23andMers869312184
23andMe allrs869312184
SNP Nexus

SNPshotrs869312184
SNPdbers869312184
MSV3drs869312184
GWAS Ctlgrs869312184
Max Magnitude0
ClinVar
Risk rs869312184(;)
Alt rs869312184(;)
Reference rs869312184(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene ABCA4
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000001.10:g.94514454delC
CLNSRC
CLNACC RCV000210324.1,