rs786201886

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CA;TAT)	6	Breast cancer associated mutation
(TAT;TAT)	0	common in clinvar

Make rs786201886(CA;CA)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108284234

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs786201886
dbSNP (classic)	rs786201886
ClinGen	rs786201886
ebi	rs786201886
HLI	rs786201886
Exac	rs786201886
Gnomad	rs786201886
Varsome	rs786201886
LitVar	rs786201886
Map	rs786201886
PheGenI	rs786201886
Biobank	rs786201886
1000 genomes	rs786201886
hgdp	rs786201886
ensembl	rs786201886
geneview	rs786201886
scholar	rs786201886
google	rs786201886
pharmgkb	rs786201886
gwascentral	rs786201886
openSNP	rs786201886
23andMe	rs786201886
SNPshot	rs786201886
SNPdbe	rs786201886
MSV3d	rs786201886
GWAS Ctlg	rs786201886

Max Magnitude

6

ClinVar
Risk	rs786201886(CA;CA)
Alt	rs786201886(CA;CA)
Reference	Rs786201886(TAT;TAT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108154961_108154963delTATinsCA
CLNSRC
CLNACC	RCV000164396.1, RCV000487413.1,