rs878854115

Orientation

plus

Stabilized

plus

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

Make rs878854115(-;-)

Make rs878854115(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

2088119

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs878854115
dbSNP (classic)	rs878854115
ClinGen	rs878854115
ebi	rs878854115
HLI	rs878854115
Exac	rs878854115
Gnomad	rs878854115
Varsome	rs878854115
LitVar	rs878854115
Map	rs878854115
PheGenI	rs878854115
Biobank	rs878854115
1000 genomes	rs878854115
hgdp	rs878854115
ensembl	rs878854115
geneview	rs878854115
scholar	rs878854115
google	rs878854115
pharmgkb	rs878854115
gwascentral	rs878854115
openSNP	rs878854115
23andMe	rs878854115
SNPshot	rs878854115
SNPdbe	rs878854115
MSV3d	rs878854115
GWAS Ctlg	rs878854115

Max Magnitude

0

ClinVar
Risk	rs878854115(-;-)
Alt	rs878854115(-;-)
Reference	Rs878854115(C;C)
Significance	Probable-Pathogenic
Disease	Tuberous sclerosis 2
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis 2
Reversed	0
HGVS	NC_000016.9:g.2138120delC
CLNSRC
CLNACC	RCV000227937.1,