rs876658878

Orientation

plus

Stabilized

plus

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

Make rs876658878(-;-)

Make rs876658878(-;AG)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

2054319

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs876658878
dbSNP (classic)	rs876658878
ClinGen	rs876658878
ebi	rs876658878
HLI	rs876658878
Exac	rs876658878
Gnomad	rs876658878
Varsome	rs876658878
LitVar	rs876658878
Map	rs876658878
PheGenI	rs876658878
Biobank	rs876658878
1000 genomes	rs876658878
hgdp	rs876658878
ensembl	rs876658878
geneview	rs876658878
scholar	rs876658878
google	rs876658878
pharmgkb	rs876658878
gwascentral	rs876658878
openSNP	rs876658878
23andMe	rs876658878
SNPshot	rs876658878
SNPdbe	rs876658878
MSV3d	rs876658878
GWAS Ctlg	rs876658878

Max Magnitude

0

ClinVar
Risk	rs876658878(-;-)
Alt	rs876658878(-;-)
Reference	Rs876658878(AG;AG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TSC2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000016.9:g.2104320_2104321delAG
CLNSRC
CLNACC	RCV000219250.1,