rs1057518508

Orientation

plus

Stabilized

plus

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

Make rs1057518508(-;-)

Make rs1057518508(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2054387

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs1057518508
dbSNP (classic)	rs1057518508
ClinGen	rs1057518508
ebi	rs1057518508
HLI	rs1057518508
Exac	rs1057518508
Gnomad	rs1057518508
Varsome	rs1057518508
LitVar	rs1057518508
Map	rs1057518508
PheGenI	rs1057518508
Biobank	rs1057518508
1000 genomes	rs1057518508
hgdp	rs1057518508
ensembl	rs1057518508
geneview	rs1057518508
scholar	rs1057518508
google	rs1057518508
pharmgkb	rs1057518508
gwascentral	rs1057518508
openSNP	rs1057518508
23andMe	rs1057518508
SNPshot	rs1057518508
SNPdbe	rs1057518508
MSV3d	rs1057518508
GWAS Ctlg	rs1057518508

Max Magnitude

0

ClinVar
Risk	rs1057518508(-;-)
Alt	rs1057518508(-;-)
Reference	Rs1057518508(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2104388delT
CLNSRC
CLNACC	RCV000413504.1,