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rs786205589

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205589(A;A)
Make rs786205589(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position54621573
GeneRP1
is asnp
is mentioned by
dbSNPrs786205589
ebirs786205589
HLIrs786205589
Exacrs786205589
Varsomers786205589
Maprs786205589
PheGenIrs786205589
hapmaprs786205589
1000 genomesrs786205589
hgdprs786205589
ensemblrs786205589
gopubmedrs786205589
geneviewrs786205589
scholarrs786205589
googlers786205589
pharmgkbrs786205589
gwascentralrs786205589
openSNPrs786205589
23andMers786205589
23andMe allrs786205589
SNP Nexus

SNPshotrs786205589
SNPdbers786205589
MSV3drs786205589
GWAS Ctlgrs786205589
Max Magnitude0
ClinVar
Risk rs786205589(A;A)
Alt rs786205589(A;A)
Reference rs786205589(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RP1
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.55534133G>A
CLNSRC
CLNACC RCV000171412.1,