rs794727906

Orientation

plus

Stabilized

plus

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

Make rs794727906(C;C)

Make rs794727906(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

2056643

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs794727906
dbSNP (classic)	rs794727906
ClinGen	rs794727906
ebi	rs794727906
HLI	rs794727906
Exac	rs794727906
Gnomad	rs794727906
Varsome	rs794727906
LitVar	rs794727906
Map	rs794727906
PheGenI	rs794727906
Biobank	rs794727906
1000 genomes	rs794727906
hgdp	rs794727906
ensembl	rs794727906
geneview	rs794727906
scholar	rs794727906
google	rs794727906
pharmgkb	rs794727906
gwascentral	rs794727906
openSNP	rs794727906
23andMe	rs794727906
SNPshot	rs794727906
SNPdbe	rs794727906
MSV3d	rs794727906
GWAS Ctlg	rs794727906

Max Magnitude

6.3

ClinVar
Risk	rs794727906(C;C)
Alt	rs794727906(C;C)
Reference	Rs794727906(G;G)
Significance	Pathogenic
Disease	Tuberous sclerosis 2
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis 2
Reversed	0
HGVS	NC_000016.9:g.2106644G>C
CLNSRC
CLNACC	RCV000180176.1,