rs1057520759

Orientation

plus

Stabilized

plus

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

Make rs1057520759(G;T)

Make rs1057520759(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2081711

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs1057520759
dbSNP (classic)	rs1057520759
ClinGen	rs1057520759
ebi	rs1057520759
HLI	rs1057520759
Exac	rs1057520759
Gnomad	rs1057520759
Varsome	rs1057520759
LitVar	rs1057520759
Map	rs1057520759
PheGenI	rs1057520759
Biobank	rs1057520759
1000 genomes	rs1057520759
hgdp	rs1057520759
ensembl	rs1057520759
geneview	rs1057520759
scholar	rs1057520759
google	rs1057520759
pharmgkb	rs1057520759
gwascentral	rs1057520759
openSNP	rs1057520759
23andMe	rs1057520759
SNPshot	rs1057520759
SNPdbe	rs1057520759
MSV3d	rs1057520759
GWAS Ctlg	rs1057520759

Max Magnitude

0

ClinVar
Risk	rs1057520759(T;T)
Alt	rs1057520759(T;T)
Reference	Rs1057520759(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2131712G>T
CLNSRC
CLNACC	RCV000434569.1,