rs137853983

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;CCT)	6.3	Tuberous Sclerosis Complex
(CTC;CTC)	0	common in clinvar

Make rs137853983(-;-)

Make rs137853983(CCT;CCT)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2062522

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs137853983
dbSNP (classic)	rs137853983
ClinGen	rs137853983
ebi	rs137853983
HLI	rs137853983
Exac	rs137853983
Gnomad	rs137853983
Varsome	rs137853983
LitVar	rs137853983
Map	rs137853983
PheGenI	rs137853983
Biobank	rs137853983
1000 genomes	rs137853983
hgdp	rs137853983
ensembl	rs137853983
geneview	rs137853983
scholar	rs137853983
google	rs137853983
pharmgkb	rs137853983
gwascentral	rs137853983
openSNP	rs137853983
23andMe	rs137853983
SNPshot	rs137853983
SNPdbe	rs137853983
MSV3d	rs137853983
GWAS Ctlg	rs137853983

Max Magnitude

6.3

ClinVar
Risk	rs137853983(-;-)
Alt	rs137853983(-;-)
Reference	Rs137853983(CTC;CTC)
Significance	Probable-Pathogenic
Disease	Tuberous sclerosis syndrome not specified Tuberous sclerosis 2
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis syndrome not specified Tuberous sclerosis 2
Reversed	0
HGVS	NC_000016.9:g.2112523_2112525delCCT
CLNSRC	Tuberous sclerosis database (TSC2)
CLNACC	RCV000042906.2, RCV000190056.1, RCV000475301.1,