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

rs1057519136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519136(-;A)
Make rs1057519136(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position79513357
GeneLCA5
is asnp
is mentioned by
dbSNPrs1057519136
dbSNP (classic)rs1057519136
ClinGenrs1057519136
ebirs1057519136
HLIrs1057519136
Exacrs1057519136
Gnomadrs1057519136
Varsomers1057519136
LitVarrs1057519136
Maprs1057519136
PheGenIrs1057519136
Biobankrs1057519136
1000 genomesrs1057519136
hgdprs1057519136
ensemblrs1057519136
geneviewrs1057519136
scholarrs1057519136
googlers1057519136
pharmgkbrs1057519136
gwascentralrs1057519136
openSNPrs1057519136
23andMers1057519136
23andMe allrs1057519136
SNPshotrs1057519136
SNPdbers1057519136
MSV3drs1057519136
GWAS Ctlgrs1057519136
Max Magnitude0
ClinVar
Risk rs1057519136(A;A)
Alt rs1057519136(A;A)
Reference Rs1057519136(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LCA5
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.80223075dupT
CLNSRC
CLNACC RCV000415875.2,