rs1057524479

Orientation

minus

Stabilized

minus

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

Make rs1057524479(C;T)

Make rs1057524479(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

37699168

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs1057524479
dbSNP (classic)	rs1057524479
ClinGen	rs1057524479
ebi	rs1057524479
HLI	rs1057524479
Exac	rs1057524479
Gnomad	rs1057524479
Varsome	rs1057524479
LitVar	rs1057524479
Map	rs1057524479
PheGenI	rs1057524479
Biobank	rs1057524479
1000 genomes	rs1057524479
hgdp	rs1057524479
ensembl	rs1057524479
geneview	rs1057524479
scholar	rs1057524479
google	rs1057524479
pharmgkb	rs1057524479
gwascentral	rs1057524479
openSNP	rs1057524479
23andMe	rs1057524479
SNPshot	rs1057524479
SNPdbe	rs1057524479
MSV3d	rs1057524479
GWAS Ctlg	rs1057524479

Max Magnitude

0

ClinVar
Risk	rs1057524479(T;T)
Alt	rs1057524479(T;T)
Reference	Rs1057524479(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HNF1B
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.36059174G>A
CLNSRC
CLNACC	RCV000429830.1,