rs869312754

Orientation

plus

Stabilized

plus

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

Make rs869312754(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108227594

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs869312754
dbSNP (classic)	rs869312754
ClinGen	rs869312754
ebi	rs869312754
HLI	rs869312754
Exac	rs869312754
Gnomad	rs869312754
Varsome	rs869312754
LitVar	rs869312754
Map	rs869312754
PheGenI	rs869312754
Biobank	rs869312754
1000 genomes	rs869312754
hgdp	rs869312754
ensembl	rs869312754
geneview	rs869312754
scholar	rs869312754
google	rs869312754
pharmgkb	rs869312754
gwascentral	rs869312754
openSNP	rs869312754
23andMe	rs869312754
SNPshot	rs869312754
SNPdbe	rs869312754
MSV3d	rs869312754
GWAS Ctlg	rs869312754

Max Magnitude

6

ClinVar
Risk	rs869312754(T;T)
Alt	rs869312754(T;T)
Reference	Rs869312754(G;G)
Significance	Probable-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.108098321G>T
CLNSRC
CLNACC	RCV000210108.1, RCV000255796.1,