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

rs587777486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777486(A;A)
Make rs587777486(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position94412370
GeneCEP83
is asnp
is mentioned by
dbSNPrs587777486
ebirs587777486
HLIrs587777486
Exacrs587777486
Varsomers587777486
Maprs587777486
PheGenIrs587777486
hapmaprs587777486
1000 genomesrs587777486
hgdprs587777486
ensemblrs587777486
gopubmedrs587777486
geneviewrs587777486
scholarrs587777486
googlers587777486
pharmgkbrs587777486
gwascentralrs587777486
openSNPrs587777486
23andMers587777486
23andMe allrs587777486
SNP Nexus

SNPshotrs587777486
SNPdbers587777486
MSV3drs587777486
GWAS Ctlgrs587777486
Max Magnitude0
ClinVar
Risk rs587777486(A;A)
Alt rs587777486(A;A)
Reference rs587777486(G;G)
Significance Pathogenic
Disease Nephronophthisis 18
Variation info
Gene CCDC41
CLNDBN Nephronophthisis 18
Reversed 0
HGVS NC_000012.11:g.94806146G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128439.2,