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rs121918039

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918039(A;A)
Make rs121918039(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position88043277
GenePKD2
is asnp
is mentioned by
dbSNPrs121918039
ebirs121918039
HLIrs121918039
Exacrs121918039
Varsomers121918039
Maprs121918039
PheGenIrs121918039
hapmaprs121918039
1000 genomesrs121918039
hgdprs121918039
ensemblrs121918039
gopubmedrs121918039
geneviewrs121918039
scholarrs121918039
googlers121918039
pharmgkbrs121918039
gwascentralrs121918039
openSNPrs121918039
23andMers121918039
23andMe allrs121918039
SNP Nexus

SNPshotrs121918039
SNPdbers121918039
MSV3drs121918039
GWAS Ctlgrs121918039
Max Magnitude0
OMIM173910
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918039(A;A)
Alt rs121918039(A;A)
Reference rs121918039(G;G)
Significance Pathogenic
Disease Polycystic kidney disease 2
Variation info
Gene PKD2
CLNDBN Polycystic kidney disease 2
Reversed 0
HGVS NC_000004.11:g.88964429G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014472.18,