rs1057519371

Orientation

minus

Stabilized

minus

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

Make rs1057519371(-;C)

Make rs1057519371(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

37710576

Gene	HNF1B, LOC105371754

is a	snp
is	mentioned by
dbSNP	rs1057519371
dbSNP (classic)	rs1057519371
ClinGen	rs1057519371
ebi	rs1057519371
HLI	rs1057519371
Exac	rs1057519371
Gnomad	rs1057519371
Varsome	rs1057519371
LitVar	rs1057519371
Map	rs1057519371
PheGenI	rs1057519371
Biobank	rs1057519371
1000 genomes	rs1057519371
hgdp	rs1057519371
ensembl	rs1057519371
geneview	rs1057519371
scholar	rs1057519371
google	rs1057519371
pharmgkb	rs1057519371
gwascentral	rs1057519371
openSNP	rs1057519371
23andMe	rs1057519371
SNPshot	rs1057519371
SNPdbe	rs1057519371
MSV3d	rs1057519371
GWAS Ctlg	rs1057519371

Max Magnitude

0

ClinVar
Risk	rs1057519371(C;C)
Alt	rs1057519371(C;C)
Reference	Rs1057519371(-;-)
Significance	Pathogenic
Disease	Familial hypoplastic
Variation	info
Gene	HNF1B
CLNDBN	Familial hypoplastic, glomerulocystic kidney
Reversed	1
HGVS	NC_000017.10:g.36070585dupG
CLNSRC
CLNACC	RCV000416588.1,