rs1060500914

Orientation

plus

Stabilized

plus

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

Make rs1060500914(-;-)

Make rs1060500914(-;TCTG)

Make rs1060500914(TCTG;TCTG)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2076089

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs1060500914
dbSNP (classic)	rs1060500914
ClinGen	rs1060500914
ebi	rs1060500914
HLI	rs1060500914
Exac	rs1060500914
Gnomad	rs1060500914
Varsome	rs1060500914
LitVar	rs1060500914
Map	rs1060500914
PheGenI	rs1060500914
Biobank	rs1060500914
1000 genomes	rs1060500914
hgdp	rs1060500914
ensembl	rs1060500914
geneview	rs1060500914
scholar	rs1060500914
google	rs1060500914
pharmgkb	rs1060500914
gwascentral	rs1060500914
openSNP	rs1060500914
23andMe	rs1060500914
SNPshot	rs1060500914
SNPdbe	rs1060500914
MSV3d	rs1060500914
GWAS Ctlg	rs1060500914

Max Magnitude

0

ClinVar
Risk	rs1060500914(-;-)
Alt	rs1060500914(-;-)
Reference	Rs1060500914(TGTC;TGTC)
Significance	Pathogenic
Disease	Tuberous sclerosis 2
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis 2
Reversed	0
HGVS	NC_000016.9:g.2126090_2126093delTCTG
CLNSRC
CLNACC	RCV000463722.1,