rs878854105

Orientation

plus

Stabilized

plus

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

Make rs878854105(-;-)

Make rs878854105(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

2084695

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs878854105
dbSNP (classic)	rs878854105
ClinGen	rs878854105
ebi	rs878854105
HLI	rs878854105
Exac	rs878854105
Gnomad	rs878854105
Varsome	rs878854105
LitVar	rs878854105
Map	rs878854105
PheGenI	rs878854105
Biobank	rs878854105
1000 genomes	rs878854105
hgdp	rs878854105
ensembl	rs878854105
geneview	rs878854105
scholar	rs878854105
google	rs878854105
pharmgkb	rs878854105
gwascentral	rs878854105
openSNP	rs878854105
23andMe	rs878854105
SNPshot	rs878854105
SNPdbe	rs878854105
MSV3d	rs878854105
GWAS Ctlg	rs878854105

Max Magnitude

0

ClinVar
Risk	rs878854105(-;-)
Alt	rs878854105(-;-)
Reference	Rs878854105(A;A)
Significance	Pathogenic
Disease	Tuberous sclerosis 2 not provided
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis 2 not provided
Reversed	0
HGVS	NC_000016.9:g.2134696delA
CLNSRC
CLNACC	RCV000233034.1, RCV000279478.1,