rs886041820

Orientation

minus

Stabilized

minus

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

Chromosome

17

Position

37739577

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs886041820
dbSNP (classic)	rs886041820
ClinGen	rs886041820
ebi	rs886041820
HLI	rs886041820
Exac	rs886041820
Gnomad	rs886041820
Varsome	rs886041820
LitVar	rs886041820
Map	rs886041820
PheGenI	rs886041820
Biobank	rs886041820
1000 genomes	rs886041820
hgdp	rs886041820
ensembl	rs886041820
geneview	rs886041820
scholar	rs886041820
google	rs886041820
pharmgkb	rs886041820
gwascentral	rs886041820
openSNP	rs886041820
23andMe	rs886041820
SNPshot	rs886041820
SNPdbe	rs886041820
MSV3d	rs886041820
GWAS Ctlg	rs886041820

Max Magnitude

0

ClinVar
Risk	rs886041820(C;C)
Alt	rs886041820(C;C)
Reference	Rs886041820(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HNF1B
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.36099569dupG
CLNSRC
CLNACC	RCV000378370.1,