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rs786205630

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205630(-;-)
Make rs786205630(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position47839760
GeneCRX
is asnp
is mentioned by
dbSNPrs786205630
ebirs786205630
HLIrs786205630
Exacrs786205630
Varsomers786205630
Maprs786205630
PheGenIrs786205630
hapmaprs786205630
1000 genomesrs786205630
hgdprs786205630
ensemblrs786205630
gopubmedrs786205630
geneviewrs786205630
scholarrs786205630
googlers786205630
pharmgkbrs786205630
gwascentralrs786205630
openSNPrs786205630
23andMers786205630
23andMe allrs786205630
SNP Nexus

SNPshotrs786205630
SNPdbers786205630
MSV3drs786205630
GWAS Ctlgrs786205630
Max Magnitude0
ClinVar
Risk rs786205630(;)
Alt rs786205630(;)
Reference rs786205630(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CRX
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.48343017delC
CLNSRC
CLNACC RCV000171490.1,