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rs587777353

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777353(C;C)
Make rs587777353(C;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position4335060
GeneGLIS2
is asnp
is mentioned by
dbSNPrs587777353
ebirs587777353
HLIrs587777353
Exacrs587777353
Varsomers587777353
Maprs587777353
PheGenIrs587777353
hapmaprs587777353
1000 genomesrs587777353
hgdprs587777353
ensemblrs587777353
gopubmedrs587777353
geneviewrs587777353
scholarrs587777353
googlers587777353
pharmgkbrs587777353
gwascentralrs587777353
openSNPrs587777353
23andMers587777353
23andMe allrs587777353
SNP Nexus

SNPshotrs587777353
SNPdbers587777353
MSV3drs587777353
GWAS Ctlgrs587777353
Max Magnitude0
ClinVar
Risk rs587777353(C;C)
Alt rs587777353(C;C)
Reference rs587777353(T;T)
Significance Pathogenic
Disease Nephronophthisis 7 Nephronophthisis
Variation info
Gene GLIS2
CLNDBN Nephronophthisis 7 Nephronophthisis
Reversed 0
HGVS NC_000016.9:g.4385061T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000115016.2, RCV000234822.1,