rs876658500

Orientation

plus

Stabilized

plus

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

Make rs876658500(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108235835

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876658500
dbSNP (classic)	rs876658500
ClinGen	rs876658500
ebi	rs876658500
HLI	rs876658500
Exac	rs876658500
Gnomad	rs876658500
Varsome	rs876658500
LitVar	rs876658500
Map	rs876658500
PheGenI	rs876658500
Biobank	rs876658500
1000 genomes	rs876658500
hgdp	rs876658500
ensembl	rs876658500
geneview	rs876658500
scholar	rs876658500
google	rs876658500
pharmgkb	rs876658500
gwascentral	rs876658500
openSNP	rs876658500
23andMe	rs876658500
SNPshot	rs876658500
SNPdbe	rs876658500
MSV3d	rs876658500
GWAS Ctlg	rs876658500

Max Magnitude

6

ClinVar
Risk	rs876658500(A;A)
Alt	rs876658500(A;A)
Reference	Rs876658500(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108106562G>A
CLNSRC
CLNACC	RCV000220072.1,