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rs786205531

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205531(A;A)
Make rs786205531(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position98396627
GeneCNGA3
is asnp
is mentioned by
dbSNPrs786205531
ebirs786205531
HLIrs786205531
Exacrs786205531
Varsomers786205531
Maprs786205531
PheGenIrs786205531
hapmaprs786205531
1000 genomesrs786205531
hgdprs786205531
ensemblrs786205531
gopubmedrs786205531
geneviewrs786205531
scholarrs786205531
googlers786205531
pharmgkbrs786205531
gwascentralrs786205531
openSNPrs786205531
23andMers786205531
23andMe allrs786205531
SNP Nexus

SNPshotrs786205531
SNPdbers786205531
MSV3drs786205531
GWAS Ctlgrs786205531
Max Magnitude0
ClinVar
Risk rs786205531(A;A)
Alt rs786205531(A;A)
Reference rs786205531(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CNGA3
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.99013090G>A
CLNSRC
CLNACC RCV000171301.1,