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

rs786205653

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205653(-;-)
Make rs786205653(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position79491666
GeneLCA5
is asnp
is mentioned by
dbSNPrs786205653
ebirs786205653
HLIrs786205653
Exacrs786205653
Varsomers786205653
Maprs786205653
PheGenIrs786205653
hapmaprs786205653
1000 genomesrs786205653
hgdprs786205653
ensemblrs786205653
gopubmedrs786205653
geneviewrs786205653
scholarrs786205653
googlers786205653
pharmgkbrs786205653
gwascentralrs786205653
openSNPrs786205653
23andMers786205653
23andMe allrs786205653
SNP Nexus

SNPshotrs786205653
SNPdbers786205653
MSV3drs786205653
GWAS Ctlgrs786205653
Max Magnitude0
ClinVar
Risk rs786205653(;)
Alt rs786205653(;)
Reference rs786205653(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LCA5
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.80201383delC
CLNSRC
CLNACC RCV000171526.1,