rs786203888

Orientation

plus

Stabilized

plus

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

Make rs786203888(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108227854

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs786203888
dbSNP (classic)	rs786203888
ClinGen	rs786203888
ebi	rs786203888
HLI	rs786203888
Exac	rs786203888
Gnomad	rs786203888
Varsome	rs786203888
LitVar	rs786203888
Map	rs786203888
PheGenI	rs786203888
Biobank	rs786203888
1000 genomes	rs786203888
hgdp	rs786203888
ensembl	rs786203888
geneview	rs786203888
scholar	rs786203888
google	rs786203888
pharmgkb	rs786203888
gwascentral	rs786203888
openSNP	rs786203888
23andMe	rs786203888
SNPshot	rs786203888
SNPdbe	rs786203888
MSV3d	rs786203888
GWAS Ctlg	rs786203888

Max Magnitude

6

ClinVar
Risk	rs786203888(T;T)
Alt	rs786203888(T;T)
Reference	Rs786203888(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.108098581C>T
CLNSRC
CLNACC	RCV000167389.1,