rs1060505021

Orientation

minus

Stabilized

minus

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

Make rs1060505021(C;T)

Make rs1060505021(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

132921872

Gene

TSC1

is a	snp
is	mentioned by
dbSNP	rs1060505021
dbSNP (classic)	rs1060505021
ClinGen	rs1060505021
ebi	rs1060505021
HLI	rs1060505021
Exac	rs1060505021
Gnomad	rs1060505021
Varsome	rs1060505021
LitVar	rs1060505021
Map	rs1060505021
PheGenI	rs1060505021
Biobank	rs1060505021
1000 genomes	rs1060505021
hgdp	rs1060505021
ensembl	rs1060505021
geneview	rs1060505021
scholar	rs1060505021
google	rs1060505021
pharmgkb	rs1060505021
gwascentral	rs1060505021
openSNP	rs1060505021
23andMe	rs1060505021
SNPshot	rs1060505021
SNPdbe	rs1060505021
MSV3d	rs1060505021
GWAS Ctlg	rs1060505021

Max Magnitude

0

ClinVar
Risk	rs1060505021(T;T)
Alt	rs1060505021(T;T)
Reference	Rs1060505021(C;C)
Significance	Pathogenic
Disease	FOCAL CORTICAL DYSPLASIA
Variation	info
Gene	TSC1
CLNDBN	FOCAL CORTICAL DYSPLASIA, TYPE II, SOMATIC
Reversed	1
HGVS	NC_000009.11:g.135797259G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000477742.1,