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rs879253769

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879253769(C;T)
Make rs879253769(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position27055171
GeneAGBL5
is asnp
is mentioned by
dbSNPrs879253769
ebirs879253769
HLIrs879253769
Exacrs879253769
Varsomers879253769
Maprs879253769
PheGenIrs879253769
hapmaprs879253769
1000 genomesrs879253769
hgdprs879253769
ensemblrs879253769
gopubmedrs879253769
geneviewrs879253769
scholarrs879253769
googlers879253769
pharmgkbrs879253769
gwascentralrs879253769
openSNPrs879253769
23andMers879253769
23andMe allrs879253769
SNP Nexus

SNPshotrs879253769
SNPdbers879253769
MSV3drs879253769
GWAS Ctlgrs879253769
Max Magnitude0
ClinVar
Risk rs879253769(T;T)
Alt rs879253769(T;T)
Reference rs879253769(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 75
Variation info
Gene AGBL5
CLNDBN Retinitis pigmentosa 75
Reversed 0
HGVS NC_000002.11:g.27278039C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000234932.1,