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rs62654395

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;G) 3 Carrier of a mutation for Stargardt disease
(G;G) 0 common in clinvar
Make rs62654395(G;T)
Make rs62654395(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position94111546
GeneABCA4
is asnp
is mentioned by
dbSNPrs62654395
dbSNP (old)rs62654395
ClinGenrs62654395
ebirs62654395
HLIrs62654395
Exacrs62654395
Varsomers62654395
Maprs62654395
PheGenIrs62654395
Biobankrs62654395
1000 genomesrs62654395
hgdprs62654395
ensemblrs62654395
gopubmedrs62654395
geneviewrs62654395
scholarrs62654395
googlers62654395
pharmgkbrs62654395
gwascentralrs62654395
openSNPrs62654395
23andMers62654395
23andMe allrs62654395
SNP Nexus

SNPshotrs62654395
SNPdbers62654395
MSV3drs62654395
GWAS Ctlgrs62654395
Max Magnitude3
ClinVar
Risk rs62654395(A;A) rs62654395(T;T)
Alt rs62654395(A;A) rs62654395(T;T)
Reference Rs62654395(G;G)
Significance Other
Disease not provided Stargardt disease 1
Variation info
Gene ABCA4
CLNDBN not provided Stargardt disease 1
Reversed 1
HGVS NC_000001.10:g.94577102C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000085451.1, RCV000132588.2,