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rs201553871

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201553871(C;C)
Make rs201553871(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position57923327
GeneCNGB1
is asnp
is mentioned by
dbSNPrs201553871
ebirs201553871
HLIrs201553871
Exacrs201553871
Varsomers201553871
Maprs201553871
PheGenIrs201553871
hapmaprs201553871
1000 genomesrs201553871
hgdprs201553871
ensemblrs201553871
gopubmedrs201553871
geneviewrs201553871
scholarrs201553871
googlers201553871
pharmgkbrs201553871
gwascentralrs201553871
openSNPrs201553871
23andMers201553871
23andMe allrs201553871
SNP Nexus

SNPshotrs201553871
SNPdbers201553871
MSV3drs201553871
GWAS Ctlgrs201553871
Max Magnitude0
ClinVar
Risk rs201553871(C;C)
Alt rs201553871(C;C)
Reference rs201553871(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 45
Variation info
Gene CNGB1
CLNDBN Retinitis pigmentosa 45
Reversed 0
HGVS NC_000016.9:g.57957231G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000191921.2,