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rs61753034

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61753034(G;G)
Make rs61753034(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position94007727
GeneABCA4
is asnp
is mentioned by
dbSNPrs61753034
ebirs61753034
HLIrs61753034
Exacrs61753034
Varsomers61753034
Maprs61753034
PheGenIrs61753034
hapmaprs61753034
1000 genomesrs61753034
hgdprs61753034
ensemblrs61753034
gopubmedrs61753034
geneviewrs61753034
scholarrs61753034
googlers61753034
pharmgkbrs61753034
gwascentralrs61753034
openSNPrs61753034
23andMers61753034
23andMe allrs61753034
SNP Nexus

SNPshotrs61753034
SNPdbers61753034
MSV3drs61753034
GWAS Ctlgrs61753034
Max Magnitude0
OMIM601691
Desc
Variant0015
Relatedalso


ClinVar
Risk rs61753034(G;G)
Alt rs61753034(G;G)
Reference rs61753034(T;T)
Significance Pathogenic
Disease Stargardt's disease not provided
Variation info
Gene ABCA4
CLNDBN Stargardt's disease not provided
Reversed 1
HGVS NC_000001.10:g.94473283A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008347.2, RCV000085774.1,