rs1057520779

Orientation

plus

Stabilized

plus

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

Make rs1057520779(A;A)

Make rs1057520779(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

120993679

Gene

HNF1A

is a	snp
is	mentioned by
dbSNP	rs1057520779
dbSNP (classic)	rs1057520779
ClinGen	rs1057520779
ebi	rs1057520779
HLI	rs1057520779
Exac	rs1057520779
Gnomad	rs1057520779
Varsome	rs1057520779
LitVar	rs1057520779
Map	rs1057520779
PheGenI	rs1057520779
Biobank	rs1057520779
1000 genomes	rs1057520779
hgdp	rs1057520779
ensembl	rs1057520779
geneview	rs1057520779
scholar	rs1057520779
google	rs1057520779
pharmgkb	rs1057520779
gwascentral	rs1057520779
openSNP	rs1057520779
23andMe	rs1057520779
SNPshot	rs1057520779
SNPdbe	rs1057520779
MSV3d	rs1057520779
GWAS Ctlg	rs1057520779

Max Magnitude

0

ClinVar
Risk	rs1057520779(A;A)
Alt	rs1057520779(A;A)
Reference	Rs1057520779(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HNF1A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.121431482G>A
CLNSRC
CLNACC	RCV000432234.1,