rs1057524790

Orientation

plus

Stabilized

plus

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

Make rs1057524790(C;C)

Make rs1057524790(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

44406234

Gene	HNF4A, MIR3646

is a	snp
is	mentioned by
dbSNP	rs1057524790
dbSNP (classic)	rs1057524790
ClinGen	rs1057524790
ebi	rs1057524790
HLI	rs1057524790
Exac	rs1057524790
Gnomad	rs1057524790
Varsome	rs1057524790
LitVar	rs1057524790
Map	rs1057524790
PheGenI	rs1057524790
Biobank	rs1057524790
1000 genomes	rs1057524790
hgdp	rs1057524790
ensembl	rs1057524790
geneview	rs1057524790
scholar	rs1057524790
google	rs1057524790
pharmgkb	rs1057524790
gwascentral	rs1057524790
openSNP	rs1057524790
23andMe	rs1057524790
SNPshot	rs1057524790
SNPdbe	rs1057524790
MSV3d	rs1057524790
GWAS Ctlg	rs1057524790

Max Magnitude

0

ClinVar
Risk	rs1057524790(C;C)
Alt	rs1057524790(C;C)
Reference	Rs1057524790(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MIR3646 HNF4A
CLNDBN	not provided
Reversed	0
HGVS	NC_000020.10:g.43034874T>C
CLNSRC
CLNACC	RCV000434164.1,