rs150513055

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3.6	Mature onset diabetes of the young (type 3)

Make rs150513055(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

120988973

Gene

HNF1A

is a	snp
is	mentioned by
dbSNP	rs150513055
dbSNP (classic)	rs150513055
ClinGen	rs150513055
ebi	rs150513055
HLI	rs150513055
Exac	rs150513055
Gnomad	rs150513055
Varsome	rs150513055
LitVar	rs150513055
Map	rs150513055
PheGenI	rs150513055
Biobank	rs150513055
1000 genomes	rs150513055
hgdp	rs150513055
ensembl	rs150513055
geneview	rs150513055
scholar	rs150513055
google	rs150513055
pharmgkb	rs150513055
gwascentral	rs150513055
openSNP	rs150513055
23andMe	rs150513055
SNPshot	rs150513055
SNPdbe	rs150513055
MSV3d	rs150513055
GWAS Ctlg	rs150513055

Max Magnitude

3.6

ClinVar
Risk	rs150513055(A;A) rs150513055(T;T)
Alt	rs150513055(A;A) rs150513055(T;T)
Reference	Rs150513055(C;C)
Significance	Probable-Pathogenic
Disease	Maturity-onset diabetes of the young
Variation	info
Gene	HNF1A
CLNDBN	Maturity-onset diabetes of the young, type 3
Reversed	0
HGVS	NC_000012.11:g.121426776C>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030503.1,