rs137853335

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	2	associated with MODY1; maturity onset of diabetes in the young (type 1)

Make rs137853335(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

44413795

Gene

HNF4A

is a	snp
is	mentioned by
dbSNP	rs137853335
dbSNP (classic)	rs137853335
ClinGen	rs137853335
ebi	rs137853335
HLI	rs137853335
Exac	rs137853335
Gnomad	rs137853335
Varsome	rs137853335
LitVar	rs137853335
Map	rs137853335
PheGenI	rs137853335
Biobank	rs137853335
1000 genomes	rs137853335
hgdp	rs137853335
ensembl	rs137853335
geneview	rs137853335
scholar	rs137853335
google	rs137853335
pharmgkb	rs137853335
gwascentral	rs137853335
openSNP	rs137853335
23andMe	rs137853335
SNPshot	rs137853335
SNPdbe	rs137853335
MSV3d	rs137853335
GWAS Ctlg	rs137853335

Max Magnitude

2

OMIM	600281
Desc
Variant	0002
Related	also

ClinVar
Risk	rs137853335(T;T)
Alt	rs137853335(T;T)
Reference	Rs137853335(C;C)
Significance	Pathogenic
Disease	Maturity-onset diabetes of the young
Variation	info
Gene	HNF4A
CLNDBN	Maturity-onset diabetes of the young, type 1
Reversed	0
HGVS	NC_000020.10:g.43042435C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009791.4,