rs786202694

Orientation

plus

Stabilized

plus

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

Make rs786202694(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108284260

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs786202694
dbSNP (classic)	rs786202694
ClinGen	rs786202694
ebi	rs786202694
HLI	rs786202694
Exac	rs786202694
Gnomad	rs786202694
Varsome	rs786202694
LitVar	rs786202694
Map	rs786202694
PheGenI	rs786202694
Biobank	rs786202694
1000 genomes	rs786202694
hgdp	rs786202694
ensembl	rs786202694
geneview	rs786202694
scholar	rs786202694
google	rs786202694
pharmgkb	rs786202694
gwascentral	rs786202694
openSNP	rs786202694
23andMe	rs786202694
SNPshot	rs786202694
SNPdbe	rs786202694
MSV3d	rs786202694
GWAS Ctlg	rs786202694

Max Magnitude

6

ClinVar
Risk	rs786202694(G;G)
Alt	rs786202694(G;G)
Reference	Rs786202694(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108154987dupG
CLNSRC
CLNACC	RCV000165632.1,