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rs786205521

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205521(A;A)
Make rs786205521(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position47839341
GeneCRX
is asnp
is mentioned by
dbSNPrs786205521
ebirs786205521
HLIrs786205521
Exacrs786205521
Varsomers786205521
Maprs786205521
PheGenIrs786205521
hapmaprs786205521
1000 genomesrs786205521
hgdprs786205521
ensemblrs786205521
gopubmedrs786205521
geneviewrs786205521
scholarrs786205521
googlers786205521
pharmgkbrs786205521
gwascentralrs786205521
openSNPrs786205521
23andMers786205521
23andMe allrs786205521
SNP Nexus

SNPshotrs786205521
SNPdbers786205521
MSV3drs786205521
GWAS Ctlgrs786205521
Max Magnitude0
ClinVar
Risk rs786205521(A;A)
Alt rs786205521(A;A)
Reference rs786205521(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CRX
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.48342598G>A
CLNSRC
CLNACC RCV000171286.1,