rs398123308

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	5	Polycystic kidney disease, autosomal dominant form (predicted)
(G;G)	0	common in clinvar

Make rs398123308(A;A)

Reference

GRCh38 38.1/141

Chromosome

4

Position

88019572

Gene

PKD2

is a	snp
is	mentioned by
dbSNP	rs398123308
dbSNP (classic)	rs398123308
ClinGen	rs398123308
ebi	rs398123308
HLI	rs398123308
Exac	rs398123308
Gnomad	rs398123308
Varsome	rs398123308
LitVar	rs398123308
Map	rs398123308
PheGenI	rs398123308
Biobank	rs398123308
1000 genomes	rs398123308
hgdp	rs398123308
ensembl	rs398123308
geneview	rs398123308
scholar	rs398123308
google	rs398123308
pharmgkb	rs398123308
gwascentral	rs398123308
openSNP	rs398123308
23andMe	rs398123308
SNPshot	rs398123308
SNPdbe	rs398123308
MSV3d	rs398123308
GWAS Ctlg	rs398123308

Max Magnitude

5

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,