rs786203370

Orientation

plus

Stabilized

plus

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

Make rs786203370(-;-)

Make rs786203370(TTCA;TTCA)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108227841

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs786203370
dbSNP (classic)	rs786203370
ClinGen	rs786203370
ebi	rs786203370
HLI	rs786203370
Exac	rs786203370
Gnomad	rs786203370
Varsome	rs786203370
LitVar	rs786203370
Map	rs786203370
PheGenI	rs786203370
Biobank	rs786203370
1000 genomes	rs786203370
hgdp	rs786203370
ensembl	rs786203370
geneview	rs786203370
scholar	rs786203370
google	rs786203370
pharmgkb	rs786203370
gwascentral	rs786203370
openSNP	rs786203370
23andMe	rs786203370
SNPshot	rs786203370
SNPdbe	rs786203370
MSV3d	rs786203370
GWAS Ctlg	rs786203370

Max Magnitude

6

ClinVar
Risk	rs786203370(-;-)
Alt	rs786203370(-;-)
Reference	Rs786203370(CATT;CATT)
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.108098568_108098571delTTCA
CLNSRC
CLNACC	RCV000166647.1, RCV000235307.2,