rs529294719

Orientation

plus

Stabilized

plus

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

Make rs529294719(C;T)

Make rs529294719(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

37733611

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs529294719
dbSNP (classic)	rs529294719
ClinGen	rs529294719
ebi	rs529294719
HLI	rs529294719
Exac	rs529294719
Gnomad	rs529294719
Varsome	rs529294719
LitVar	rs529294719
Map	rs529294719
PheGenI	rs529294719
Biobank	rs529294719
1000 genomes	rs529294719
hgdp	rs529294719
ensembl	rs529294719
geneview	rs529294719
scholar	rs529294719
google	rs529294719
pharmgkb	rs529294719
gwascentral	rs529294719
openSNP	rs529294719
23andMe	rs529294719
SNPshot	rs529294719
SNPdbe	rs529294719
MSV3d	rs529294719
GWAS Ctlg	rs529294719

Max Magnitude

0

ClinVar
Risk	rs529294719(G;G) rs529294719(T;T)
Alt	rs529294719(G;G) rs529294719(T;T)
Reference	Rs529294719(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HNF1B
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.36093604C>G
CLNSRC
CLNACC	RCV000479017.1,