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rs398123307

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123307(A;A)
Make rs398123307(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position88057990
GenePKD2
is asnp
is mentioned by
dbSNPrs398123307
ebirs398123307
HLIrs398123307
Exacrs398123307
Varsomers398123307
Maprs398123307
PheGenIrs398123307
hapmaprs398123307
1000 genomesrs398123307
hgdprs398123307
ensemblrs398123307
gopubmedrs398123307
geneviewrs398123307
scholarrs398123307
googlers398123307
pharmgkbrs398123307
gwascentralrs398123307
openSNPrs398123307
23andMers398123307
23andMe allrs398123307
SNP Nexus

SNPshotrs398123307
SNPdbers398123307
MSV3drs398123307
GWAS Ctlgrs398123307
Max Magnitude0
ClinVar
Risk rs398123307(A;A)
Alt rs398123307(A;A)
Reference rs398123307(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKD2
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.88979142C>A
CLNSRC ClinVar Emory University
CLNACC RCV000078581.4,