rs1057519220

Orientation

minus

Stabilized

minus

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

Make rs1057519220(C;T)

Make rs1057519220(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

2169670

Gene

TH

is a	snp
is	mentioned by
dbSNP	rs1057519220
dbSNP (classic)	rs1057519220
ClinGen	rs1057519220
ebi	rs1057519220
HLI	rs1057519220
Exac	rs1057519220
Gnomad	rs1057519220
Varsome	rs1057519220
LitVar	rs1057519220
Map	rs1057519220
PheGenI	rs1057519220
Biobank	rs1057519220
1000 genomes	rs1057519220
hgdp	rs1057519220
ensembl	rs1057519220
geneview	rs1057519220
scholar	rs1057519220
google	rs1057519220
pharmgkb	rs1057519220
gwascentral	rs1057519220
openSNP	rs1057519220
23andMe	rs1057519220
SNPshot	rs1057519220
SNPdbe	rs1057519220
MSV3d	rs1057519220
GWAS Ctlg	rs1057519220

Max Magnitude

0

ClinVar
Risk	rs1057519220(T;T)
Alt	rs1057519220(T;T)
Reference	Rs1057519220(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TH
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.2190900G>A
CLNSRC
CLNACC	RCV000415910.2,