Have questions? Visit https://www.reddit.com/r/SNPedia

rs387907310

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907310(C;T)
Make rs387907310(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position117351872
GeneCEP164
is asnp
is mentioned by
dbSNPrs387907310
ebirs387907310
HLIrs387907310
Exacrs387907310
Varsomers387907310
Maprs387907310
PheGenIrs387907310
hapmaprs387907310
1000 genomesrs387907310
hgdprs387907310
ensemblrs387907310
gopubmedrs387907310
geneviewrs387907310
scholarrs387907310
googlers387907310
pharmgkbrs387907310
gwascentralrs387907310
openSNPrs387907310
23andMers387907310
23andMe allrs387907310
SNP Nexus

SNPshotrs387907310
SNPdbers387907310
MSV3drs387907310
GWAS Ctlgrs387907310
Max Magnitude0
ClinVar
Risk rs387907310(T;T)
Alt rs387907310(T;T)
Reference rs387907310(C;C)
Significance Pathogenic
Disease Nephronophthisis 15
Variation info
Gene CEP164
CLNDBN Nephronophthisis 15
Reversed 0
HGVS NC_000011.9:g.117222588C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030835.3,