rs759520465

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs759520465(C;C)

Make rs759520465(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108292618

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs759520465
dbSNP (classic)	rs759520465
ClinGen	rs759520465
ebi	rs759520465
HLI	rs759520465
Exac	rs759520465
Gnomad	rs759520465
Varsome	rs759520465
LitVar	rs759520465
Map	rs759520465
PheGenI	rs759520465
Biobank	rs759520465
1000 genomes	rs759520465
hgdp	rs759520465
ensembl	rs759520465
geneview	rs759520465
scholar	rs759520465
google	rs759520465
pharmgkb	rs759520465
gwascentral	rs759520465
openSNP	rs759520465
23andMe	rs759520465
SNPshot	rs759520465
SNPdbe	rs759520465
MSV3d	rs759520465
GWAS Ctlg	rs759520465

Max Magnitude

0

ClinVar
Risk	rs759520465(A;A) rs759520465(C;C)
Alt	rs759520465(A;A) rs759520465(C;C)
Reference	Rs759520465(G;G)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108163345G>A; NC_000011.9:g.108163345G>C
CLNSRC
CLNACC	RCV000255051.1, RCV000216400.1, RCV000486776.1,