rs796053506

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(D;D)	0	common genotype

Make rs796053506(-;C)

Make rs796053506(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

2081722

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs796053506
dbSNP (classic)	rs796053506
ClinGen	rs796053506
ebi	rs796053506
HLI	rs796053506
Exac	rs796053506
Gnomad	rs796053506
Varsome	rs796053506
LitVar	rs796053506
Map	rs796053506
PheGenI	rs796053506
Biobank	rs796053506
1000 genomes	rs796053506
hgdp	rs796053506
ensembl	rs796053506
geneview	rs796053506
scholar	rs796053506
google	rs796053506
pharmgkb	rs796053506
gwascentral	rs796053506
openSNP	rs796053506
23andMe	rs796053506
SNPshot	rs796053506
SNPdbe	rs796053506
MSV3d	rs796053506
GWAS Ctlg	rs796053506

Max Magnitude

0

ClinVar
Risk	rs796053506(C;C)
Alt	rs796053506(C;C)
Reference	Rs796053506(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2131723dupC
CLNSRC
CLNACC	RCV000190063.1,