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rs61748552

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61748552(C;G)
Make rs61748552(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position94078611
GeneABCA4
is asnp
is mentioned by
dbSNPrs61748552
ebirs61748552
HLIrs61748552
Exacrs61748552
Varsomers61748552
Maprs61748552
PheGenIrs61748552
hapmaprs61748552
1000 genomesrs61748552
hgdprs61748552
ensemblrs61748552
gopubmedrs61748552
geneviewrs61748552
scholarrs61748552
googlers61748552
pharmgkbrs61748552
gwascentralrs61748552
openSNPrs61748552
23andMers61748552
23andMe allrs61748552
SNP Nexus

SNPshotrs61748552
SNPdbers61748552
MSV3drs61748552
GWAS Ctlgrs61748552
Max Magnitude0
ClinVar
Risk rs61748552(G;G)
Alt rs61748552(G;G)
Reference rs61748552(C;C)
Significance Probable-Pathogenic
Disease not provided Retinal dystrophy
Variation info
Gene ABCA4
CLNDBN not provided Retinal dystrophy
Reversed 1
HGVS NC_000001.10:g.94544167G>C
CLNSRC
CLNACC RCV000085388.1, RCV000210294.1,