rs786202608

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;T)	6	Breast cancer associated mutation
(I;I)	0	common genotype
(T;T)	0	common in clinvar

Make rs786202608(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108268525

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs786202608
dbSNP (classic)	rs786202608
ClinGen	rs786202608
ebi	rs786202608
HLI	rs786202608
Exac	rs786202608
Gnomad	rs786202608
Varsome	rs786202608
LitVar	rs786202608
Map	rs786202608
PheGenI	rs786202608
Biobank	rs786202608
1000 genomes	rs786202608
hgdp	rs786202608
ensembl	rs786202608
geneview	rs786202608
scholar	rs786202608
google	rs786202608
pharmgkb	rs786202608
gwascentral	rs786202608
openSNP	rs786202608
23andMe	rs786202608
SNPshot	rs786202608
SNPdbe	rs786202608
MSV3d	rs786202608
GWAS Ctlg	rs786202608

Max Magnitude

6

ClinVar
Risk	rs786202608(-;-)
Alt	rs786202608(-;-)
Reference	Rs786202608(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108139252delT
CLNSRC
CLNACC	RCV000165502.1, RCV000466400.1,