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rs878855332

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855332(-;-)
Make rs878855332(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position100253089
GeneINVS
is asnp
is mentioned by
dbSNPrs878855332
ebirs878855332
HLIrs878855332
Exacrs878855332
Varsomers878855332
Maprs878855332
PheGenIrs878855332
hapmaprs878855332
1000 genomesrs878855332
hgdprs878855332
ensemblrs878855332
gopubmedrs878855332
geneviewrs878855332
scholarrs878855332
googlers878855332
pharmgkbrs878855332
gwascentralrs878855332
openSNPrs878855332
23andMers878855332
23andMe allrs878855332
SNP Nexus

SNPshotrs878855332
SNPdbers878855332
MSV3drs878855332
GWAS Ctlgrs878855332
Max Magnitude0
ClinVar
Risk rs878855332(;)
Alt rs878855332(;)
Reference rs878855332(G;G)
Significance Pathogenic
Disease Nephronophthisis
Variation info
Gene INVS
CLNDBN Nephronophthisis
Reversed 0
HGVS NC_000009.11:g.103015371delG
CLNSRC
CLNACC RCV000234834.1,