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rs398124500

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124500(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position51753327
GenePKHD1
is asnp
is mentioned by
dbSNPrs398124500
ebirs398124500
HLIrs398124500
Exacrs398124500
Varsomers398124500
Maprs398124500
PheGenIrs398124500
hapmaprs398124500
1000 genomesrs398124500
hgdprs398124500
ensemblrs398124500
gopubmedrs398124500
geneviewrs398124500
scholarrs398124500
googlers398124500
pharmgkbrs398124500
gwascentralrs398124500
openSNPrs398124500
23andMers398124500
23andMe allrs398124500
SNP Nexus

SNPshotrs398124500
SNPdbers398124500
MSV3drs398124500
GWAS Ctlgrs398124500
Max Magnitude0
ClinVar
Risk rs398124500(T;T)
Alt rs398124500(T;T)
Reference rs398124500(C;C)
Significance Other
Disease not provided Polycystic kidney disease
Variation info
Gene PKHD1
CLNDBN not provided Polycystic kidney disease, infantile type
Reversed 1
HGVS NC_000006.11:g.51618125G>A
CLNSRC HGMD
CLNACC RCV000082589.3, RCV000169555.2,