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rs387907311

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907311(C;T)
Make rs387907311(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position117381864
GeneCEP164
is asnp
is mentioned by
dbSNPrs387907311
ebirs387907311
HLIrs387907311
Exacrs387907311
Varsomers387907311
Maprs387907311
PheGenIrs387907311
hapmaprs387907311
1000 genomesrs387907311
hgdprs387907311
ensemblrs387907311
gopubmedrs387907311
geneviewrs387907311
scholarrs387907311
googlers387907311
pharmgkbrs387907311
gwascentralrs387907311
openSNPrs387907311
23andMers387907311
23andMe allrs387907311
SNP Nexus

SNPshotrs387907311
SNPdbers387907311
MSV3drs387907311
GWAS Ctlgrs387907311
Max Magnitude0
ClinVar
Risk rs387907311(T;T)
Alt rs387907311(T;T)
Reference rs387907311(C;C)
Significance Pathogenic
Disease Nephronophthisis 15
Variation info
Gene CEP164
CLNDBN Nephronophthisis 15
Reversed 0
HGVS NC_000011.9:g.117252580C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030836.4,