rs137853241

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	2	associated with MODY3; maturity onset of diabetes in the young (type 3)

Make rs137853241(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

121001155

Gene

HNF1A

is a	snp
is	mentioned by
dbSNP	rs137853241
dbSNP (classic)	rs137853241
ClinGen	rs137853241
ebi	rs137853241
HLI	rs137853241
Exac	rs137853241
Gnomad	rs137853241
Varsome	rs137853241
LitVar	rs137853241
Map	rs137853241
PheGenI	rs137853241
Biobank	rs137853241
1000 genomes	rs137853241
hgdp	rs137853241
ensembl	rs137853241
geneview	rs137853241
scholar	rs137853241
google	rs137853241
pharmgkb	rs137853241
gwascentral	rs137853241
openSNP	rs137853241
23andMe	rs137853241
SNPshot	rs137853241
SNPdbe	rs137853241
MSV3d	rs137853241
GWAS Ctlg	rs137853241

Max Magnitude

2

OMIM	142410
Desc
Variant	0009
Related	also

ClinVar
Risk	rs137853241(T;T)
Alt	rs137853241(T;T)
Reference	Rs137853241(C;C)
Significance	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.121438958C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016072.25,