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rs745770404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs745770404(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position52050157
GenePKHD1
is asnp
is mentioned by
dbSNPrs745770404
ebirs745770404
HLIrs745770404
Exacrs745770404
Varsomers745770404
Maprs745770404
PheGenIrs745770404
hapmaprs745770404
1000 genomesrs745770404
hgdprs745770404
ensemblrs745770404
gopubmedrs745770404
geneviewrs745770404
scholarrs745770404
googlers745770404
pharmgkbrs745770404
gwascentralrs745770404
openSNPrs745770404
23andMers745770404
23andMe allrs745770404
SNP Nexus

SNPshotrs745770404
SNPdbers745770404
MSV3drs745770404
GWAS Ctlgrs745770404
Max Magnitude0
ClinVar
Risk rs745770404(T;T)
Alt rs745770404(T;T)
Reference rs745770404(C;C)
Significance Probable-Pathogenic
Disease Polycystic kidney disease
Variation info
Gene PKHD1
CLNDBN Polycystic kidney disease, infantile type
Reversed 0
HGVS NC_000006.11:g.51914955C>T
CLNSRC
CLNACC RCV000169230.1,