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rs786205532

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205532(A;A)
Make rs786205532(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position98396743
GeneCNGA3
is asnp
is mentioned by
dbSNPrs786205532
ebirs786205532
HLIrs786205532
Exacrs786205532
Varsomers786205532
Maprs786205532
PheGenIrs786205532
hapmaprs786205532
1000 genomesrs786205532
hgdprs786205532
ensemblrs786205532
gopubmedrs786205532
geneviewrs786205532
scholarrs786205532
googlers786205532
pharmgkbrs786205532
gwascentralrs786205532
openSNPrs786205532
23andMers786205532
23andMe allrs786205532
SNP Nexus

SNPshotrs786205532
SNPdbers786205532
MSV3drs786205532
GWAS Ctlgrs786205532
Max Magnitude0
ClinVar
Risk rs786205532(A;A)
Alt rs786205532(A;A)
Reference rs786205532(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CNGA3
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.99013206G>A
CLNSRC
CLNACC RCV000171302.1,