Have questions? Visit https://www.reddit.com/r/SNPedia

rs879255251

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs879255251(-;GGCCCGGCGCGGCCCC)
Make rs879255251(GGCCCGGCGCGGCCCC;GGCCCGGCGCGGCCCC)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position123373635
GeneCRB2
is asnp
is mentioned by
dbSNPrs879255251
ClinGenrs879255251
ebirs879255251
HLIrs879255251
Exacrs879255251
Varsomers879255251
Maprs879255251
PheGenIrs879255251
hapmaprs879255251
1000 genomesrs879255251
hgdprs879255251
ensemblrs879255251
gopubmedrs879255251
geneviewrs879255251
scholarrs879255251
googlers879255251
pharmgkbrs879255251
gwascentralrs879255251
openSNPrs879255251
23andMers879255251
23andMe allrs879255251
SNP Nexus

SNPshotrs879255251
SNPdbers879255251
MSV3drs879255251
GWAS Ctlgrs879255251
Max Magnitude0
ClinVar
Risk rs879255251(GGCGCGGCCCCGGCCC;GGCGCGGCCCCGGCCC)
Alt rs879255251(GGCGCGGCCCCGGCCC;GGCGCGGCCCCGGCCC)
Reference Rs879255251(-;-)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 9 not provided
Variation info
Gene CRB2
CLNDBN Focal segmental glomerulosclerosis 9 not provided
Reversed 0
HGVS NC_000009.11:g.126135899_126135914dup16
CLNSRC OMIM Allelic Variant
CLNACC RCV000157656.3, RCV000481736.1,