rs1057520291

Orientation

plus

Stabilized

plus

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

Make rs1057520291(C;T)

Make rs1057520291(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

120989017

Gene

HNF1A

is a	snp
is	mentioned by
dbSNP	rs1057520291
dbSNP (classic)	rs1057520291
ClinGen	rs1057520291
ebi	rs1057520291
HLI	rs1057520291
Exac	rs1057520291
Gnomad	rs1057520291
Varsome	rs1057520291
LitVar	rs1057520291
Map	rs1057520291
PheGenI	rs1057520291
Biobank	rs1057520291
1000 genomes	rs1057520291
hgdp	rs1057520291
ensembl	rs1057520291
geneview	rs1057520291
scholar	rs1057520291
google	rs1057520291
pharmgkb	rs1057520291
gwascentral	rs1057520291
openSNP	rs1057520291
23andMe	rs1057520291
SNPshot	rs1057520291
SNPdbe	rs1057520291
MSV3d	rs1057520291
GWAS Ctlg	rs1057520291

Max Magnitude

0

ClinVar
Risk	rs1057520291(T;T)
Alt	rs1057520291(T;T)
Reference	Rs1057520291(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HNF1A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.121426820C>T
CLNSRC
CLNACC	RCV000436030.1,