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rs757470958

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757470958(A;A)
Make rs757470958(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position98380207
GeneCNGA3
is asnp
is mentioned by
dbSNPrs757470958
ebirs757470958
HLIrs757470958
Exacrs757470958
Varsomers757470958
Maprs757470958
PheGenIrs757470958
hapmaprs757470958
1000 genomesrs757470958
hgdprs757470958
ensemblrs757470958
gopubmedrs757470958
geneviewrs757470958
scholarrs757470958
googlers757470958
pharmgkbrs757470958
gwascentralrs757470958
openSNPrs757470958
23andMers757470958
23andMe allrs757470958
SNP Nexus

SNPshotrs757470958
SNPdbers757470958
MSV3drs757470958
GWAS Ctlgrs757470958
Max Magnitude0
ClinVar
Risk rs757470958(A;A)
Alt rs757470958(A;A)
Reference rs757470958(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CNGA3
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000002.11:g.98996670G>A
CLNSRC
CLNACC RCV000225523.1,