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rs879253768

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879253768(A;A)
Make rs879253768(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position27055228
GeneAGBL5
is asnp
is mentioned by
dbSNPrs879253768
ebirs879253768
HLIrs879253768
Exacrs879253768
Varsomers879253768
Maprs879253768
PheGenIrs879253768
hapmaprs879253768
1000 genomesrs879253768
hgdprs879253768
ensemblrs879253768
gopubmedrs879253768
geneviewrs879253768
scholarrs879253768
googlers879253768
pharmgkbrs879253768
gwascentralrs879253768
openSNPrs879253768
23andMers879253768
23andMe allrs879253768
SNP Nexus

SNPshotrs879253768
SNPdbers879253768
MSV3drs879253768
GWAS Ctlgrs879253768
Max Magnitude0
ClinVar
Risk rs879253768(A;A)
Alt rs879253768(A;A)
Reference rs879253768(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 75
Variation info
Gene AGBL5
CLNDBN Retinitis pigmentosa 75
Reversed 0
HGVS NC_000002.11:g.27278096G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000234931.1,