rs137854028

Orientation

plus

Stabilized

plus

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

Make rs137854028(-;-)

Make rs137854028(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2084994

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs137854028
dbSNP (classic)	rs137854028
ClinGen	rs137854028
ebi	rs137854028
HLI	rs137854028
Exac	rs137854028
Gnomad	rs137854028
Varsome	rs137854028
LitVar	rs137854028
Map	rs137854028
PheGenI	rs137854028
Biobank	rs137854028
1000 genomes	rs137854028
hgdp	rs137854028
ensembl	rs137854028
geneview	rs137854028
scholar	rs137854028
google	rs137854028
pharmgkb	rs137854028
gwascentral	rs137854028
openSNP	rs137854028
23andMe	rs137854028
SNPshot	rs137854028
SNPdbe	rs137854028
MSV3d	rs137854028
GWAS Ctlg	rs137854028

Max Magnitude

0

ClinVar
Risk	rs137854028(-;-)
Alt	rs137854028(-;-)
Reference	Rs137854028(G;G)
Significance	Pathogenic
Disease	Tuberous sclerosis syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000016.9:g.2134995delG
CLNSRC	Tuberous sclerosis database (TSC2)
CLNACC	RCV000042765.2, RCV000491824.1,