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rs145646425

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145646425(C;T)
Make rs145646425(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position117387204
GeneCEP164
is asnp
is mentioned by
dbSNPrs145646425
ebirs145646425
HLIrs145646425
Exacrs145646425
Varsomers145646425
Maprs145646425
PheGenIrs145646425
hapmaprs145646425
1000 genomesrs145646425
hgdprs145646425
ensemblrs145646425
gopubmedrs145646425
geneviewrs145646425
scholarrs145646425
googlers145646425
pharmgkbrs145646425
gwascentralrs145646425
openSNPrs145646425
23andMers145646425
23andMe allrs145646425
SNP Nexus

SNPshotrs145646425
SNPdbers145646425
MSV3drs145646425
GWAS Ctlgrs145646425
Max Magnitude0
ClinVar
Risk rs145646425(T;T)
Alt rs145646425(T;T)
Reference rs145646425(C;C)
Significance Pathogenic
Disease Nephronophthisis 15
Variation info
Gene CEP164
CLNDBN Nephronophthisis 15
Reversed 0
HGVS NC_000011.9:g.117257920C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030837.3,