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rs398123308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123308(A;A)
Make rs398123308(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position88019572
GenePKD2
is asnp
is mentioned by
dbSNPrs398123308
ebirs398123308
HLIrs398123308
Exacrs398123308
Varsomers398123308
Maprs398123308
PheGenIrs398123308
hapmaprs398123308
1000 genomesrs398123308
hgdprs398123308
ensemblrs398123308
gopubmedrs398123308
geneviewrs398123308
scholarrs398123308
googlers398123308
pharmgkbrs398123308
gwascentralrs398123308
openSNPrs398123308
23andMers398123308
23andMe allrs398123308
SNP Nexus

SNPshotrs398123308
SNPdbers398123308
MSV3drs398123308
GWAS Ctlgrs398123308
Max Magnitude0
ClinVar
Risk rs398123308(A;A)
Alt rs398123308(A;A)
Reference rs398123308(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PKD2
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.88940724G>A
CLNSRC HGMD
CLNACC RCV000078584.4,