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rs372504780

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372504780(A;A)
Make rs372504780(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position57950463
GeneCNGB1
is asnp
is mentioned by
dbSNPrs372504780
ebirs372504780
HLIrs372504780
Exacrs372504780
Varsomers372504780
Maprs372504780
PheGenIrs372504780
hapmaprs372504780
1000 genomesrs372504780
hgdprs372504780
ensemblrs372504780
gopubmedrs372504780
geneviewrs372504780
scholarrs372504780
googlers372504780
pharmgkbrs372504780
gwascentralrs372504780
openSNPrs372504780
23andMers372504780
23andMe allrs372504780
SNP Nexus

SNPshotrs372504780
SNPdbers372504780
MSV3drs372504780
GWAS Ctlgrs372504780
Max Magnitude0
ClinVar
Risk rs372504780(A;A)
Alt rs372504780(A;A)
Reference rs372504780(G;G)
Significance Pathogenic
Disease not provided Retinitis pigmentosa 45
Variation info
Gene CNGB1
CLNDBN not provided Retinitis pigmentosa 45
Reversed 0
HGVS NC_000016.9:g.57984367G>A
CLNSRC ClinVar
CLNACC RCV000079637.3, RCV000174506.1,