rs137853977

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;AT)	6.3	Tuberous Sclerosis Complex
(AT;AT)	0	common in clinvar

Make rs137853977(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

2057156

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs137853977
dbSNP (classic)	rs137853977
ClinGen	rs137853977
ebi	rs137853977
HLI	rs137853977
Exac	rs137853977
Gnomad	rs137853977
Varsome	rs137853977
LitVar	rs137853977
Map	rs137853977
PheGenI	rs137853977
Biobank	rs137853977
1000 genomes	rs137853977
hgdp	rs137853977
ensembl	rs137853977
geneview	rs137853977
scholar	rs137853977
google	rs137853977
pharmgkb	rs137853977
gwascentral	rs137853977
openSNP	rs137853977
23andMe	rs137853977
SNPshot	rs137853977
SNPdbe	rs137853977
MSV3d	rs137853977
GWAS Ctlg	rs137853977

Max Magnitude

6.3

ClinVar
Risk	rs137853977(-;-)
Alt	rs137853977(-;-)
Reference	Rs137853977(AT;AT)
Significance	Pathogenic
Disease	Tuberous sclerosis syndrome Tuberous sclerosis 2 not provided
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis syndrome Tuberous sclerosis 2 not provided
Reversed	0
HGVS	NC_000016.9:g.2107157_2107158delAT
CLNSRC	Tuberous sclerosis database (TSC2)
CLNACC	RCV000042707.2, RCV000180518.2, RCV000312270.1,