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rs878855335

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855335(G;T)
Make rs878855335(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position4335394
GeneGLIS2
is asnp
is mentioned by
dbSNPrs878855335
ebirs878855335
HLIrs878855335
Exacrs878855335
Varsomers878855335
Maprs878855335
PheGenIrs878855335
hapmaprs878855335
1000 genomesrs878855335
hgdprs878855335
ensemblrs878855335
gopubmedrs878855335
geneviewrs878855335
scholarrs878855335
googlers878855335
pharmgkbrs878855335
gwascentralrs878855335
openSNPrs878855335
23andMers878855335
23andMe allrs878855335
SNP Nexus

SNPshotrs878855335
SNPdbers878855335
MSV3drs878855335
GWAS Ctlgrs878855335
Max Magnitude0
ClinVar
Risk rs878855335(T;T)
Alt rs878855335(T;T)
Reference rs878855335(G;G)
Significance Pathogenic
Disease Nephronophthisis
Variation info
Gene GLIS2
CLNDBN Nephronophthisis
Reversed 0
HGVS NC_000016.9:g.4385395G>T
CLNSRC
CLNACC RCV000234831.1,