rs1057523727

Orientation

plus

Stabilized

plus

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

Make rs1057523727(C;C)

Make rs1057523727(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2060813

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs1057523727
dbSNP (classic)	rs1057523727
ClinGen	rs1057523727
ebi	rs1057523727
HLI	rs1057523727
Exac	rs1057523727
Gnomad	rs1057523727
Varsome	rs1057523727
LitVar	rs1057523727
Map	rs1057523727
PheGenI	rs1057523727
Biobank	rs1057523727
1000 genomes	rs1057523727
hgdp	rs1057523727
ensembl	rs1057523727
geneview	rs1057523727
scholar	rs1057523727
google	rs1057523727
pharmgkb	rs1057523727
gwascentral	rs1057523727
openSNP	rs1057523727
23andMe	rs1057523727
SNPshot	rs1057523727
SNPdbe	rs1057523727
MSV3d	rs1057523727
GWAS Ctlg	rs1057523727

Max Magnitude

0

ClinVar
Risk	rs1057523727(C;C)
Alt	rs1057523727(C;C)
Reference	Rs1057523727(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2110814G>C
CLNSRC
CLNACC	RCV000445030.1,