rs1057517744

Orientation

minus

Stabilized

minus

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

Make rs1057517744(C;T)

Make rs1057517744(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

37739443

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs1057517744
dbSNP (classic)	rs1057517744
ClinGen	rs1057517744
ebi	rs1057517744
HLI	rs1057517744
Exac	rs1057517744
Gnomad	rs1057517744
Varsome	rs1057517744
LitVar	rs1057517744
Map	rs1057517744
PheGenI	rs1057517744
Biobank	rs1057517744
1000 genomes	rs1057517744
hgdp	rs1057517744
ensembl	rs1057517744
geneview	rs1057517744
scholar	rs1057517744
google	rs1057517744
pharmgkb	rs1057517744
gwascentral	rs1057517744
openSNP	rs1057517744
23andMe	rs1057517744
SNPshot	rs1057517744
SNPdbe	rs1057517744
MSV3d	rs1057517744
GWAS Ctlg	rs1057517744

Max Magnitude

0

ClinVar
Risk	rs1057517744(T;T)
Alt	rs1057517744(T;T)
Reference	Rs1057517744(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HNF1B
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.36099434G>A
CLNSRC
CLNACC	RCV000413356.1,