rs1057518959

Orientation

minus

Stabilized

minus

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

Make rs1057518959(C;C)

Make rs1057518959(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2091794

Gene	LOC105371049, MIR1225, PKD1

is a	snp
is	mentioned by
dbSNP	rs1057518959
dbSNP (classic)	rs1057518959
ClinGen	rs1057518959
ebi	rs1057518959
HLI	rs1057518959
Exac	rs1057518959
Gnomad	rs1057518959
Varsome	rs1057518959
LitVar	rs1057518959
Map	rs1057518959
PheGenI	rs1057518959
Biobank	rs1057518959
1000 genomes	rs1057518959
hgdp	rs1057518959
ensembl	rs1057518959
geneview	rs1057518959
scholar	rs1057518959
google	rs1057518959
pharmgkb	rs1057518959
gwascentral	rs1057518959
openSNP	rs1057518959
23andMe	rs1057518959
SNPshot	rs1057518959
SNPdbe	rs1057518959
MSV3d	rs1057518959
GWAS Ctlg	rs1057518959

Max Magnitude

0

ClinVar
Risk	rs1057518959(C;C)
Alt	rs1057518959(C;C)
Reference	Rs1057518959(T;T)
Significance	Probable-Pathogenic
Disease	Hypertension Polycystic kidney dysplasia
Variation	info
Gene	PKD1 MIR1225 LOC105371049
CLNDBN	Hypertension Polycystic kidney dysplasia
Reversed	1
HGVS	NC_000016.9:g.2141795A>G
CLNSRC
CLNACC	RCV000415211.1,