rs796053516

Orientation

plus

Stabilized

plus

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

Make rs796053516(-;-)

Make rs796053516(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

2081720

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs796053516
dbSNP (classic)	rs796053516
ClinGen	rs796053516
ebi	rs796053516
HLI	rs796053516
Exac	rs796053516
Gnomad	rs796053516
Varsome	rs796053516
LitVar	rs796053516
Map	rs796053516
PheGenI	rs796053516
Biobank	rs796053516
1000 genomes	rs796053516
hgdp	rs796053516
ensembl	rs796053516
geneview	rs796053516
scholar	rs796053516
google	rs796053516
pharmgkb	rs796053516
gwascentral	rs796053516
openSNP	rs796053516
23andMe	rs796053516
SNPshot	rs796053516
SNPdbe	rs796053516
MSV3d	rs796053516
GWAS Ctlg	rs796053516

Max Magnitude

0

ClinVar
Risk	rs796053516(-;-)
Alt	rs796053516(-;-)
Reference	Rs796053516(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2131721delG
CLNSRC
CLNACC	RCV000190085.1,