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rs121918041

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918041(C;T)
Make rs121918041(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position88043351
GenePKD2
is asnp
is mentioned by
dbSNPrs121918041
ebirs121918041
HLIrs121918041
Exacrs121918041
Varsomers121918041
Maprs121918041
PheGenIrs121918041
hapmaprs121918041
1000 genomesrs121918041
hgdprs121918041
ensemblrs121918041
gopubmedrs121918041
geneviewrs121918041
scholarrs121918041
googlers121918041
pharmgkbrs121918041
gwascentralrs121918041
openSNPrs121918041
23andMers121918041
23andMe allrs121918041
SNP Nexus

SNPshotrs121918041
SNPdbers121918041
MSV3drs121918041
GWAS Ctlgrs121918041
Max Magnitude0
OMIM173910
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918041(T;T)
Alt rs121918041(T;T)
Reference rs121918041(C;C)
Significance Pathogenic
Disease Polycystic kidney disease 2
Variation info
Gene PKD2
CLNDBN Polycystic kidney disease 2
Reversed 0
HGVS NC_000004.11:g.88964503C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014474.26,