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rs369925690

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 6 Polycystic Kidney disease
(C;T) 3 carrier of an autosomal recessive polycystic kidney disease mutation
(T;T) 0 common/normal
ReferenceGRCh38 38.1/142
Chromosome6
Position52071009
GenePKHD1
is asnp
is mentioned by
dbSNPrs369925690
ebirs369925690
HLIrs369925690
Exacrs369925690
Varsomers369925690
Maprs369925690
PheGenIrs369925690
hapmaprs369925690
1000 genomesrs369925690
hgdprs369925690
ensemblrs369925690
gopubmedrs369925690
geneviewrs369925690
scholarrs369925690
googlers369925690
pharmgkbrs369925690
gwascentralrs369925690
openSNPrs369925690
23andMers369925690
23andMe allrs369925690
SNP Nexus

SNPshotrs369925690
SNPdbers369925690
MSV3drs369925690
GWAS Ctlgrs369925690
Max Magnitude6

rs369925690, also known as c.664A>G, I222V or p.Ile222Val, is a SNP in the PKHD1 gene on chromosome 6.

The risk allele, rs369925690(C), is considered causative for autosomal recessive Polycystic kidney disease.

This SNP is referred to as i5000047 by 23andMe.