rs1060499600

Orientation

plus

Stabilized

plus

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

Make rs1060499600(-;-)

Make rs1060499600(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108244947

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs1060499600
dbSNP (classic)	rs1060499600
ClinGen	rs1060499600
ebi	rs1060499600
HLI	rs1060499600
Exac	rs1060499600
Gnomad	rs1060499600
Varsome	rs1060499600
LitVar	rs1060499600
Map	rs1060499600
PheGenI	rs1060499600
Biobank	rs1060499600
1000 genomes	rs1060499600
hgdp	rs1060499600
ensembl	rs1060499600
geneview	rs1060499600
scholar	rs1060499600
google	rs1060499600
pharmgkb	rs1060499600
gwascentral	rs1060499600
openSNP	rs1060499600
23andMe	rs1060499600
SNPshot	rs1060499600
SNPdbe	rs1060499600
MSV3d	rs1060499600
GWAS Ctlg	rs1060499600

Max Magnitude

0

ClinVar
Risk	rs1060499600(-;-)
Alt	rs1060499600(-;-)
Reference	Rs1060499600(T;T)
Significance	Pathogenic
Disease	Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108115676delT
CLNSRC
CLNACC	RCV000205636.2, RCV000221322.2,