rs137854036

Orientation

plus

Stabilized

plus

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

Make rs137854036(-;-)

Make rs137854036(-;TG)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2088139

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs137854036
dbSNP (classic)	rs137854036
ClinGen	rs137854036
ebi	rs137854036
HLI	rs137854036
Exac	rs137854036
Gnomad	rs137854036
Varsome	rs137854036
LitVar	rs137854036
Map	rs137854036
PheGenI	rs137854036
Biobank	rs137854036
1000 genomes	rs137854036
hgdp	rs137854036
ensembl	rs137854036
geneview	rs137854036
scholar	rs137854036
google	rs137854036
pharmgkb	rs137854036
gwascentral	rs137854036
openSNP	rs137854036
23andMe	rs137854036
SNPshot	rs137854036
SNPdbe	rs137854036
MSV3d	rs137854036
GWAS Ctlg	rs137854036

Max Magnitude

0

ClinVar
Risk	rs137854036(-;-)
Alt	rs137854036(-;-)
Reference	Rs137854036(TG;TG)
Significance	Pathogenic
Disease	Tuberous sclerosis syndrome not provided
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis syndrome not provided
Reversed	0
HGVS	NC_000016.9:g.2138142_2138143delTG
CLNSRC	Tuberous sclerosis database (TSC2)
CLNACC	RCV000043252.2, RCV000489070.1,