rs137854076

Orientation

plus

Stabilized

plus

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

Make rs137854076(-;-)

Make rs137854076(-;TG)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

2079350

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs137854076
dbSNP (classic)	rs137854076
ClinGen	rs137854076
ebi	rs137854076
HLI	rs137854076
Exac	rs137854076
Gnomad	rs137854076
Varsome	rs137854076
LitVar	rs137854076
Map	rs137854076
PheGenI	rs137854076
Biobank	rs137854076
1000 genomes	rs137854076
hgdp	rs137854076
ensembl	rs137854076
geneview	rs137854076
scholar	rs137854076
google	rs137854076
pharmgkb	rs137854076
gwascentral	rs137854076
openSNP	rs137854076
23andMe	rs137854076
SNPshot	rs137854076
SNPdbe	rs137854076
MSV3d	rs137854076
GWAS Ctlg	rs137854076

Max Magnitude

0

ClinVar
Risk	rs137854076(-;-)
Alt	rs137854076(-;-)
Reference	Rs137854076(TG;TG)
Significance	Pathogenic
Disease	Tuberous sclerosis syndrome Tuberous sclerosis 2
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis syndrome Tuberous sclerosis 2
Reversed	0
HGVS	NC_000016.9:g.2129351_2129352delTG
CLNSRC	Tuberous sclerosis database (TSC2)
CLNACC	RCV000042505.2, RCV000201154.1,