rs1057522911

Orientation

plus

Stabilized

plus

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

Make rs1057522911(C;C)

Make rs1057522911(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2074372

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs1057522911
dbSNP (classic)	rs1057522911
ClinGen	rs1057522911
ebi	rs1057522911
HLI	rs1057522911
Exac	rs1057522911
Gnomad	rs1057522911
Varsome	rs1057522911
LitVar	rs1057522911
Map	rs1057522911
PheGenI	rs1057522911
Biobank	rs1057522911
1000 genomes	rs1057522911
hgdp	rs1057522911
ensembl	rs1057522911
geneview	rs1057522911
scholar	rs1057522911
google	rs1057522911
pharmgkb	rs1057522911
gwascentral	rs1057522911
openSNP	rs1057522911
23andMe	rs1057522911
SNPshot	rs1057522911
SNPdbe	rs1057522911
MSV3d	rs1057522911
GWAS Ctlg	rs1057522911

Max Magnitude

0

ClinVar
Risk	rs1057522911(C;C)
Alt	rs1057522911(C;C)
Reference	Rs1057522911(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2124373T>C
CLNSRC
CLNACC	RCV000433607.1,