rs1057520783

Orientation

plus

Stabilized

plus

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

Make rs1057520783(G;G)

Make rs1057520783(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

126615469

Gene	LMX1B, LOC105376277

is a	snp
is	mentioned by
dbSNP	rs1057520783
dbSNP (classic)	rs1057520783
ClinGen	rs1057520783
ebi	rs1057520783
HLI	rs1057520783
Exac	rs1057520783
Gnomad	rs1057520783
Varsome	rs1057520783
LitVar	rs1057520783
Map	rs1057520783
PheGenI	rs1057520783
Biobank	rs1057520783
1000 genomes	rs1057520783
hgdp	rs1057520783
ensembl	rs1057520783
geneview	rs1057520783
scholar	rs1057520783
google	rs1057520783
pharmgkb	rs1057520783
gwascentral	rs1057520783
openSNP	rs1057520783
23andMe	rs1057520783
SNPshot	rs1057520783
SNPdbe	rs1057520783
MSV3d	rs1057520783
GWAS Ctlg	rs1057520783

Max Magnitude

0

ClinVar
Risk	rs1057520783(G;G)
Alt	rs1057520783(G;G)
Reference	Rs1057520783(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LMX1B
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.129377748T>G
CLNSRC
CLNACC	RCV000421725.1,