rs9296669

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs9296669(A;A)

Make rs9296669(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

52026025

Gene

PKHD1

is a	snp
is	mentioned by
dbSNP	rs9296669
dbSNP (classic)	rs9296669
ClinGen	rs9296669
ebi	rs9296669
HLI	rs9296669
Exac	rs9296669
Gnomad	rs9296669
Varsome	rs9296669
LitVar	rs9296669
Map	rs9296669
PheGenI	rs9296669
Biobank	rs9296669
1000 genomes	rs9296669
hgdp	rs9296669
ensembl	rs9296669
geneview	rs9296669
scholar	rs9296669
google	rs9296669
pharmgkb	rs9296669
gwascentral	rs9296669
openSNP	rs9296669
23andMe	rs9296669
SNPshot	rs9296669
SNPdbe	rs9296669
MSV3d	rs9296669
GWAS Ctlg	rs9296669

GMAF

0.3972

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs9296669(A;A)
Alt	rs9296669(A;A)
Reference	Rs9296669(G;G)
Significance	Non-pathogenic
Disease	not specified Autosomal recessive polycystic kidney disease
Variation	info
Gene	PKHD1
CLNDBN	not specified Autosomal recessive polycystic kidney disease
Reversed	0
HGVS	NC_000006.11:g.51890823G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000082549.6, RCV000282648.1,