rs137853237

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	3.6	Maturity onset of diabetes of the young (type 3)

Make rs137853237(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

120988871

Gene

HNF1A

is a	snp
is	mentioned by
dbSNP	rs137853237
dbSNP (classic)	rs137853237
ClinGen	rs137853237
ebi	rs137853237
HLI	rs137853237
Exac	rs137853237
Gnomad	rs137853237
Varsome	rs137853237
LitVar	rs137853237
Map	rs137853237
PheGenI	rs137853237
Biobank	rs137853237
1000 genomes	rs137853237
hgdp	rs137853237
ensembl	rs137853237
geneview	rs137853237
scholar	rs137853237
google	rs137853237
pharmgkb	rs137853237
gwascentral	rs137853237
openSNP	rs137853237
23andMe	rs137853237
SNPshot	rs137853237
SNPdbe	rs137853237
MSV3d	rs137853237
GWAS Ctlg	rs137853237

Max Magnitude

3.6

OMIM	142410
Desc
Variant	0004
Related	also

ClinVar
Risk	rs137853237(G;G)
Alt	rs137853237(G;G)
Reference	Rs137853237(A;A)
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.121426674A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016067.22,