rs121918673

Orientation

minus

Stabilized

minus

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

Make rs121918673(C;G)

Make rs121918673(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

37701122

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs121918673
dbSNP (classic)	rs121918673
ClinGen	rs121918673
ebi	rs121918673
HLI	rs121918673
Exac	rs121918673
Gnomad	rs121918673
Varsome	rs121918673
LitVar	rs121918673
Map	rs121918673
PheGenI	rs121918673
Biobank	rs121918673
1000 genomes	rs121918673
hgdp	rs121918673
ensembl	rs121918673
geneview	rs121918673
scholar	rs121918673
google	rs121918673
pharmgkb	rs121918673
gwascentral	rs121918673
openSNP	rs121918673
23andMe	rs121918673
SNPshot	rs121918673
SNPdbe	rs121918673
MSV3d	rs121918673
GWAS Ctlg	rs121918673

Max Magnitude

0

OMIM	189907
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121918673(G;G)
Alt	rs121918673(G;G)
Reference	Rs121918673(C;C)
Significance	Pathogenic
Disease	Diabetes mellitus type 2
Variation	info
Gene	HNF1B
CLNDBN	Diabetes mellitus type 2
Reversed	1
HGVS	NC_000017.10:g.36061127G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013476.22,