rs142204928

Orientation

plus

Stabilized

plus

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

Make rs142204928(A;A)

Make rs142204928(A;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

44414519

Gene

HNF4A

is a	snp
is	mentioned by
dbSNP	rs142204928
dbSNP (classic)	rs142204928
ClinGen	rs142204928
ebi	rs142204928
HLI	rs142204928
Exac	rs142204928
Gnomad	rs142204928
Varsome	rs142204928
LitVar	rs142204928
Map	rs142204928
PheGenI	rs142204928
Biobank	rs142204928
1000 genomes	rs142204928
hgdp	rs142204928
ensembl	rs142204928
geneview	rs142204928
scholar	rs142204928
google	rs142204928
pharmgkb	rs142204928
gwascentral	rs142204928
openSNP	rs142204928
23andMe	rs142204928
SNPshot	rs142204928
SNPdbe	rs142204928
MSV3d	rs142204928
GWAS Ctlg	rs142204928

GMAF

0.001837

Max Magnitude

0

ClinVar
Risk	rs142204928(A;A)
Alt	rs142204928(A;A)
Reference	Rs142204928(G;G)
Significance	Probable-non-pathogenic
Disease	Maturity-onset diabetes of the young not provided Hyperinsulinism Maturity-onset diabetes of the young Diabetes mellitus type 2
Variation	info
Gene	HNF4A
CLNDBN	Maturity-onset diabetes of the young, type 1 not provided Hyperinsulinism, Dominant Maturity-onset diabetes of the young Diabetes mellitus type 2
Reversed	0
HGVS	NC_000020.10:g.43043159G>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030023.2, RCV000117239.1, RCV000340715.1, RCV000393684.1, RCV000490471.1,