rs1060501711

Orientation

plus

Stabilized

plus

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

Make rs1060501711(A;A)

Make rs1060501711(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108279526

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs1060501711
dbSNP (classic)	rs1060501711
ClinGen	rs1060501711
ebi	rs1060501711
HLI	rs1060501711
Exac	rs1060501711
Gnomad	rs1060501711
Varsome	rs1060501711
LitVar	rs1060501711
Map	rs1060501711
PheGenI	rs1060501711
Biobank	rs1060501711
1000 genomes	rs1060501711
hgdp	rs1060501711
ensembl	rs1060501711
geneview	rs1060501711
scholar	rs1060501711
google	rs1060501711
pharmgkb	rs1060501711
gwascentral	rs1060501711
openSNP	rs1060501711
23andMe	rs1060501711
SNPshot	rs1060501711
SNPdbe	rs1060501711
MSV3d	rs1060501711
GWAS Ctlg	rs1060501711

Max Magnitude

0

ClinVar
Risk	rs1060501711(A;A)
Alt	rs1060501711(A;A)
Reference	Rs1060501711(T;T)
Significance	Pathogenic
Disease	Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108150253T>A
CLNSRC
CLNACC	RCV000460640.1, RCV000485900.1,