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rs878855333

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878855333(-;-)
Make rs878855333(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position100300601
GeneINVS
is asnp
is mentioned by
dbSNPrs878855333
ebirs878855333
HLIrs878855333
Exacrs878855333
Varsomers878855333
Maprs878855333
PheGenIrs878855333
hapmaprs878855333
1000 genomesrs878855333
hgdprs878855333
ensemblrs878855333
gopubmedrs878855333
geneviewrs878855333
scholarrs878855333
googlers878855333
pharmgkbrs878855333
gwascentralrs878855333
openSNPrs878855333
23andMers878855333
23andMe allrs878855333
SNP Nexus

SNPshotrs878855333
SNPdbers878855333
MSV3drs878855333
GWAS Ctlgrs878855333
Max Magnitude0
ClinVar
Risk rs878855333(;)
Alt rs878855333(;)
Reference rs878855333(A;A)
Significance Pathogenic
Disease Nephronophthisis
Variation info
Gene INVS
CLNDBN Nephronophthisis
Reversed 0
HGVS NC_000009.11:g.103062883delA
CLNSRC
CLNACC RCV000234816.1,