rs786203807

Orientation

plus

Stabilized

plus

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

Make rs786203807(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108256219

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs786203807
dbSNP (classic)	rs786203807
ClinGen	rs786203807
ebi	rs786203807
HLI	rs786203807
Exac	rs786203807
Gnomad	rs786203807
Varsome	rs786203807
LitVar	rs786203807
Map	rs786203807
PheGenI	rs786203807
Biobank	rs786203807
1000 genomes	rs786203807
hgdp	rs786203807
ensembl	rs786203807
geneview	rs786203807
scholar	rs786203807
google	rs786203807
pharmgkb	rs786203807
gwascentral	rs786203807
openSNP	rs786203807
23andMe	rs786203807
SNPshot	rs786203807
SNPdbe	rs786203807
MSV3d	rs786203807
GWAS Ctlg	rs786203807

Max Magnitude

6

ClinVar
Risk	rs786203807(-;-)
Alt	rs786203807(-;-)
Reference	Rs786203807(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108126946delC
CLNSRC
CLNACC	RCV000167269.1,