rs1060499575

Orientation

plus

Stabilized

plus

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

Make rs1060499575(-;-)

Make rs1060499575(-;GTGA)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108343372

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs1060499575
dbSNP (classic)	rs1060499575
ClinGen	rs1060499575
ebi	rs1060499575
HLI	rs1060499575
Exac	rs1060499575
Gnomad	rs1060499575
Varsome	rs1060499575
LitVar	rs1060499575
Map	rs1060499575
PheGenI	rs1060499575
Biobank	rs1060499575
1000 genomes	rs1060499575
hgdp	rs1060499575
ensembl	rs1060499575
geneview	rs1060499575
scholar	rs1060499575
google	rs1060499575
pharmgkb	rs1060499575
gwascentral	rs1060499575
openSNP	rs1060499575
23andMe	rs1060499575
SNPshot	rs1060499575
SNPdbe	rs1060499575
MSV3d	rs1060499575
GWAS Ctlg	rs1060499575

Max Magnitude

0

ClinVar
Risk	rs1060499575(-;-)
Alt	rs1060499575(-;-)
Reference	Rs1060499575(GTGA;GTGA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108214103_108214106delGTGA
CLNSRC
CLNACC	RCV000159624.5, RCV000204238.4, RCV000212083.2,