rs137854023

Orientation

plus

Stabilized

plus

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

Make rs137854023(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

2064391

Gene

TSC2

is a	snp
is	mentioned by
dbSNP	rs137854023
dbSNP (classic)	rs137854023
ClinGen	rs137854023
ebi	rs137854023
HLI	rs137854023
Exac	rs137854023
Gnomad	rs137854023
Varsome	rs137854023
LitVar	rs137854023
Map	rs137854023
PheGenI	rs137854023
Biobank	rs137854023
1000 genomes	rs137854023
hgdp	rs137854023
ensembl	rs137854023
geneview	rs137854023
scholar	rs137854023
google	rs137854023
pharmgkb	rs137854023
gwascentral	rs137854023
openSNP	rs137854023
23andMe	rs137854023
SNPshot	rs137854023
SNPdbe	rs137854023
MSV3d	rs137854023
GWAS Ctlg	rs137854023

Max Magnitude

6.3

ClinVar
Risk	rs137854023(A;A)
Alt	rs137854023(A;A)
Reference	Rs137854023(-;-)
Significance	Pathogenic
Disease	Tuberous sclerosis syndrome not provided
Variation	info
Gene	TSC2
CLNDBN	Tuberous sclerosis syndrome not provided
Reversed	0
HGVS	NC_000016.9:g.2114392dupA
CLNSRC	Tuberous sclerosis database (TSC2)
CLNACC	RCV000043401.2, RCV000484376.1,