rs1057517745

Orientation

plus

Stabilized

plus

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

Make rs1057517745(A;A)

Make rs1057517745(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

44406196

Gene	HNF4A, MIR3646

is a	snp
is	mentioned by
dbSNP	rs1057517745
dbSNP (classic)	rs1057517745
ClinGen	rs1057517745
ebi	rs1057517745
HLI	rs1057517745
Exac	rs1057517745
Gnomad	rs1057517745
Varsome	rs1057517745
LitVar	rs1057517745
Map	rs1057517745
PheGenI	rs1057517745
Biobank	rs1057517745
1000 genomes	rs1057517745
hgdp	rs1057517745
ensembl	rs1057517745
geneview	rs1057517745
scholar	rs1057517745
google	rs1057517745
pharmgkb	rs1057517745
gwascentral	rs1057517745
openSNP	rs1057517745
23andMe	rs1057517745
SNPshot	rs1057517745
SNPdbe	rs1057517745
MSV3d	rs1057517745
GWAS Ctlg	rs1057517745

Max Magnitude

0

ClinVar
Risk	rs1057517745(A;A)
Alt	rs1057517745(A;A)
Reference	Rs1057517745(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MIR3646 HNF4A
CLNDBN	not provided
Reversed	0
HGVS	NC_000020.10:g.43034836G>A
CLNSRC
CLNACC	RCV000414001.1,