rs1060500938

Orientation

plus

Stabilized

plus

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

Make rs1060500938(-;-)

Make rs1060500938(-;CT)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2074383

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs1060500938
dbSNP (classic)	rs1060500938
ClinGen	rs1060500938
ebi	rs1060500938
HLI	rs1060500938
Exac	rs1060500938
Gnomad	rs1060500938
Varsome	rs1060500938
LitVar	rs1060500938
Map	rs1060500938
PheGenI	rs1060500938
Biobank	rs1060500938
1000 genomes	rs1060500938
hgdp	rs1060500938
ensembl	rs1060500938
geneview	rs1060500938
scholar	rs1060500938
google	rs1060500938
pharmgkb	rs1060500938
gwascentral	rs1060500938
openSNP	rs1060500938
23andMe	rs1060500938
SNPshot	rs1060500938
SNPdbe	rs1060500938
MSV3d	rs1060500938
GWAS Ctlg	rs1060500938

Max Magnitude

0

ClinVar
Risk	rs1060500938(-;-)
Alt	rs1060500938(-;-)
Reference	Rs1060500938(CT;CT)
Significance	Pathogenic
Disease	Tuberous sclerosis 2
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis 2
Reversed	0
HGVS	NC_000016.9:g.2124384_2124385delCT
CLNSRC
CLNACC	RCV000473256.1,