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rs879255252

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255252(C;C)
Make rs879255252(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position123370939
GeneCRB2
is asnp
is mentioned by
dbSNPrs879255252
dbSNP (classic)rs879255252
ClinGenrs879255252
ebirs879255252
HLIrs879255252
Exacrs879255252
Gnomadrs879255252
Varsomers879255252
LitVarrs879255252
Maprs879255252
PheGenIrs879255252
Biobankrs879255252
1000 genomesrs879255252
hgdprs879255252
ensemblrs879255252
geneviewrs879255252
scholarrs879255252
googlers879255252
pharmgkbrs879255252
gwascentralrs879255252
openSNPrs879255252
23andMers879255252
SNPshotrs879255252
SNPdbers879255252
MSV3drs879255252
GWAS Ctlgrs879255252
Max Magnitude0
ClinVar
Risk rs879255252(C;C)
Alt rs879255252(C;C)
Reference Rs879255252(G;G)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 9
Variation info
Gene CRB2
CLNDBN Focal segmental glomerulosclerosis 9
Reversed 0
HGVS NC_000009.11:g.126133218G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000157657.3,