rs786204088

Orientation

plus

Stabilized

plus

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

Make rs786204088(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108227697

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs786204088
dbSNP (classic)	rs786204088
ClinGen	rs786204088
ebi	rs786204088
HLI	rs786204088
Exac	rs786204088
Gnomad	rs786204088
Varsome	rs786204088
LitVar	rs786204088
Map	rs786204088
PheGenI	rs786204088
Biobank	rs786204088
1000 genomes	rs786204088
hgdp	rs786204088
ensembl	rs786204088
geneview	rs786204088
scholar	rs786204088
google	rs786204088
pharmgkb	rs786204088
gwascentral	rs786204088
openSNP	rs786204088
23andMe	rs786204088
SNPshot	rs786204088
SNPdbe	rs786204088
MSV3d	rs786204088
GWAS Ctlg	rs786204088

Max Magnitude

6

ClinVar
Risk	rs786204088(A;A)
Alt	rs786204088(A;A)
Reference	Rs786204088(G;G)
Significance	Probable-Pathogenic
Disease	Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108098424G>A
CLNSRC
CLNACC	RCV000167987.1,