rs1057520384

Orientation

minus

Stabilized

minus

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

Make rs1057520384(C;T)

Make rs1057520384(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

2166003

Gene

TH

is a	snp
is	mentioned by
dbSNP	rs1057520384
dbSNP (classic)	rs1057520384
ClinGen	rs1057520384
ebi	rs1057520384
HLI	rs1057520384
Exac	rs1057520384
Gnomad	rs1057520384
Varsome	rs1057520384
LitVar	rs1057520384
Map	rs1057520384
PheGenI	rs1057520384
Biobank	rs1057520384
1000 genomes	rs1057520384
hgdp	rs1057520384
ensembl	rs1057520384
geneview	rs1057520384
scholar	rs1057520384
google	rs1057520384
pharmgkb	rs1057520384
gwascentral	rs1057520384
openSNP	rs1057520384
23andMe	rs1057520384
SNPshot	rs1057520384
SNPdbe	rs1057520384
MSV3d	rs1057520384
GWAS Ctlg	rs1057520384

Max Magnitude

0

ClinVar
Risk	rs1057520384(T;T)
Alt	rs1057520384(T;T)
Reference	Rs1057520384(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TH
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.2187233G>A
CLNSRC
CLNACC	RCV000433260.1,