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rs754392766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar


Make rs754392766(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position52058355
GenePKHD1
is asnp
is mentioned by
dbSNPrs754392766
ebirs754392766
HLIrs754392766
Exacrs754392766
Varsomers754392766
Maprs754392766
PheGenIrs754392766
hapmaprs754392766
1000 genomesrs754392766
hgdprs754392766
ensemblrs754392766
gopubmedrs754392766
geneviewrs754392766
scholarrs754392766
googlers754392766
pharmgkbrs754392766
gwascentralrs754392766
openSNPrs754392766
23andMers754392766
23andMe allrs754392766
SNP Nexus

SNPshotrs754392766
SNPdbers754392766
MSV3drs754392766
GWAS Ctlgrs754392766
Max Magnitude0
ClinVar
Risk rs754392766(A;A)
Alt rs754392766(A;A)
Reference rs754392766(G;G)
Significance Probable-Pathogenic
Disease Polycystic kidney disease
Variation info
Gene PKHD1
CLNDBN Polycystic kidney disease, infantile type
Reversed 0
HGVS NC_000006.11:g.51923153G>A
CLNSRC
CLNACC RCV000169415.1,