rs137854015

Orientation

plus

Stabilized

plus

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

Make rs137854015(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2079163

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs137854015
dbSNP (classic)	rs137854015
ClinGen	rs137854015
ebi	rs137854015
HLI	rs137854015
Exac	rs137854015
Gnomad	rs137854015
Varsome	rs137854015
LitVar	rs137854015
Map	rs137854015
PheGenI	rs137854015
Biobank	rs137854015
1000 genomes	rs137854015
hgdp	rs137854015
ensembl	rs137854015
geneview	rs137854015
scholar	rs137854015
google	rs137854015
pharmgkb	rs137854015
gwascentral	rs137854015
openSNP	rs137854015
23andMe	rs137854015
SNPshot	rs137854015
SNPdbe	rs137854015
MSV3d	rs137854015
GWAS Ctlg	rs137854015

Max Magnitude

6.3

ClinVar
Risk	rs137854015(A;A)
Alt	rs137854015(A;A)
Reference	Rs137854015(-;-)
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.2129164dupA
CLNSRC	Tuberous sclerosis database (TSC2)
CLNACC	RCV000042998.2, RCV000484132.1,