rs796053484

Orientation

plus

Stabilized

plus

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

Make rs796053484(G;T)

Make rs796053484(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

2062497

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs796053484
dbSNP (classic)	rs796053484
ClinGen	rs796053484
ebi	rs796053484
HLI	rs796053484
Exac	rs796053484
Gnomad	rs796053484
Varsome	rs796053484
LitVar	rs796053484
Map	rs796053484
PheGenI	rs796053484
Biobank	rs796053484
1000 genomes	rs796053484
hgdp	rs796053484
ensembl	rs796053484
geneview	rs796053484
scholar	rs796053484
google	rs796053484
pharmgkb	rs796053484
gwascentral	rs796053484
openSNP	rs796053484
23andMe	rs796053484
SNPshot	rs796053484
SNPdbe	rs796053484
MSV3d	rs796053484
GWAS Ctlg	rs796053484

Max Magnitude

0

ClinVar
Risk	rs796053484(C;C) rs796053484(T;T)
Alt	rs796053484(C;C) rs796053484(T;T)
Reference	Rs796053484(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.2112498G>T
CLNSRC
CLNACC	RCV000189977.1,