Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518955

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518955(-;G)
Make rs1057518955(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position94019602
GeneABCA4
is asnp
is mentioned by
dbSNPrs1057518955
dbSNP (old)rs1057518955
ClinGenrs1057518955
ebirs1057518955
HLIrs1057518955
Exacrs1057518955
Gnomadrs1057518955
Varsomers1057518955
Maprs1057518955
PheGenIrs1057518955
Biobankrs1057518955
1000 genomesrs1057518955
hgdprs1057518955
ensemblrs1057518955
gopubmedrs1057518955
geneviewrs1057518955
scholarrs1057518955
googlers1057518955
pharmgkbrs1057518955
gwascentralrs1057518955
openSNPrs1057518955
23andMers1057518955
23andMe allrs1057518955
SNPshotrs1057518955
SNPdbers1057518955
MSV3drs1057518955
GWAS Ctlgrs1057518955
Max Magnitude0
ClinVar
Risk rs1057518955(G;G)
Alt rs1057518955(G;G)
Reference Rs1057518955(-;-)
Significance Pathogenic
Disease Retinopathy Visual impairment
Variation info
Gene ABCA4
CLNDBN Retinopathy Visual impairment
Reversed 1
HGVS NC_000001.10:g.94485159dupC
CLNSRC
CLNACC RCV000414893.1,