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rs199584830

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199584830(A;A)
Make rs199584830(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position47936954
GeneCNGA1, LOC101927157
is asnp
is mentioned by
dbSNPrs199584830
ebirs199584830
HLIrs199584830
Exacrs199584830
Varsomers199584830
Maprs199584830
PheGenIrs199584830
hapmaprs199584830
1000 genomesrs199584830
hgdprs199584830
ensemblrs199584830
gopubmedrs199584830
geneviewrs199584830
scholarrs199584830
googlers199584830
pharmgkbrs199584830
gwascentralrs199584830
openSNPrs199584830
23andMers199584830
23andMe allrs199584830
SNP Nexus

SNPshotrs199584830
SNPdbers199584830
MSV3drs199584830
GWAS Ctlgrs199584830
Max Magnitude0
ClinVar
Risk rs199584830(A;A)
Alt rs199584830(A;A)
Reference rs199584830(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CNGA1 LOC101927157
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000004.11:g.47938971G>A
CLNSRC
CLNACC RCV000225417.1,