rs193922472

Orientation

plus

Stabilized

plus

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

Make rs193922472(A;G)

Make rs193922472(G;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

44413735

Gene

HNF4A

is a	snp
is	mentioned by
dbSNP	rs193922472
dbSNP (classic)	rs193922472
ClinGen	rs193922472
ebi	rs193922472
HLI	rs193922472
Exac	rs193922472
Gnomad	rs193922472
Varsome	rs193922472
LitVar	rs193922472
Map	rs193922472
PheGenI	rs193922472
Biobank	rs193922472
1000 genomes	rs193922472
hgdp	rs193922472
ensembl	rs193922472
geneview	rs193922472
scholar	rs193922472
google	rs193922472
pharmgkb	rs193922472
gwascentral	rs193922472
openSNP	rs193922472
23andMe	rs193922472
SNPshot	rs193922472
SNPdbe	rs193922472
MSV3d	rs193922472
GWAS Ctlg	rs193922472

Max Magnitude

0

ClinVar
Risk	rs193922472(G;G)
Alt	rs193922472(G;G)
Reference	Rs193922472(A;A)
Significance	Probable-Pathogenic
Disease	Maturity-onset diabetes of the young not specified
Variation	info
Gene	HNF4A
CLNDBN	Maturity-onset diabetes of the young, type 1 not specified
Reversed	0
HGVS	NC_000020.10:g.43042375A>G
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030019.1, RCV000484752.1,