rs193922477

Orientation

plus

Stabilized

plus

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

Make rs193922477(C;C)

Make rs193922477(C;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

44419818

Gene

HNF4A

is a	snp
is	mentioned by
dbSNP	rs193922477
dbSNP (classic)	rs193922477
ClinGen	rs193922477
ebi	rs193922477
HLI	rs193922477
Exac	rs193922477
Gnomad	rs193922477
Varsome	rs193922477
LitVar	rs193922477
Map	rs193922477
PheGenI	rs193922477
Biobank	rs193922477
1000 genomes	rs193922477
hgdp	rs193922477
ensembl	rs193922477
geneview	rs193922477
scholar	rs193922477
google	rs193922477
pharmgkb	rs193922477
gwascentral	rs193922477
openSNP	rs193922477
23andMe	rs193922477
SNPshot	rs193922477
SNPdbe	rs193922477
MSV3d	rs193922477
GWAS Ctlg	rs193922477

Max Magnitude

0

ClinVar
Risk	rs193922477(C;C)
Alt	rs193922477(C;C)
Reference	Rs193922477(G;G)
Significance	Probable-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.43048458G>C
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030030.1,