rs137854071

Orientation

plus

Stabilized

plus

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

Make rs137854071(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

2071908

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs137854071
dbSNP (classic)	rs137854071
ClinGen	rs137854071
ebi	rs137854071
HLI	rs137854071
Exac	rs137854071
Gnomad	rs137854071
Varsome	rs137854071
LitVar	rs137854071
Map	rs137854071
PheGenI	rs137854071
Biobank	rs137854071
1000 genomes	rs137854071
hgdp	rs137854071
ensembl	rs137854071
geneview	rs137854071
scholar	rs137854071
google	rs137854071
pharmgkb	rs137854071
gwascentral	rs137854071
openSNP	rs137854071
23andMe	rs137854071
SNPshot	rs137854071
SNPdbe	rs137854071
MSV3d	rs137854071
GWAS Ctlg	rs137854071

Max Magnitude

6.3

ClinVar
Risk	rs137854071(-;-)
Alt	rs137854071(-;-)
Reference	Rs137854071(C;C)
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.2121909delC
CLNSRC	Tuberous sclerosis database (TSC2)
CLNACC	RCV000042979.2, RCV000190058.1,