rs759183842

Orientation

plus

Stabilized

plus

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

Make rs759183842(C;C)

Make rs759183842(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

132925736

Gene

TSC1

is a	snp
is	mentioned by
dbSNP	rs759183842
dbSNP (classic)	rs759183842
ClinGen	rs759183842
ebi	rs759183842
HLI	rs759183842
Exac	rs759183842
Gnomad	rs759183842
Varsome	rs759183842
LitVar	rs759183842
Map	rs759183842
PheGenI	rs759183842
Biobank	rs759183842
1000 genomes	rs759183842
hgdp	rs759183842
ensembl	rs759183842
geneview	rs759183842
scholar	rs759183842
google	rs759183842
pharmgkb	rs759183842
gwascentral	rs759183842
openSNP	rs759183842
23andMe	rs759183842
SNPshot	rs759183842
SNPdbe	rs759183842
MSV3d	rs759183842
GWAS Ctlg	rs759183842

Max Magnitude

0

ClinVar
Risk	rs759183842(A;A) rs759183842(C;C)
Alt	rs759183842(A;A) rs759183842(C;C)
Reference	Rs759183842(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TSC1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.135801123G>C
CLNSRC
CLNACC	RCV000189832.1,