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rs61751388

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61751388(G;T)
Make rs61751388(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position94029444
GeneABCA4
is asnp
is mentioned by
dbSNPrs61751388
ebirs61751388
HLIrs61751388
Exacrs61751388
Varsomers61751388
Maprs61751388
PheGenIrs61751388
hapmaprs61751388
1000 genomesrs61751388
hgdprs61751388
ensemblrs61751388
gopubmedrs61751388
geneviewrs61751388
scholarrs61751388
googlers61751388
pharmgkbrs61751388
gwascentralrs61751388
openSNPrs61751388
23andMers61751388
23andMe allrs61751388
SNP Nexus

SNPshotrs61751388
SNPdbers61751388
MSV3drs61751388
GWAS Ctlgrs61751388
Max Magnitude0
ClinVar
Risk rs61751388(T;T)
Alt rs61751388(T;T)
Reference rs61751388(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 19 Cone-rod dystrophy 3 not provided
Variation info
Gene ABCA4
CLNDBN Retinitis pigmentosa 19 Cone-rod dystrophy 3 not provided
Reversed 1
HGVS NC_000001.10:g.94495000C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008343.3, RCV000008344.4, RCV000085647.1,