rs1057518965

Orientation

plus

Stabilized

plus

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

Make rs1057518965(-;-)

Make rs1057518965(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108244812

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs1057518965
dbSNP (classic)	rs1057518965
ClinGen	rs1057518965
ebi	rs1057518965
HLI	rs1057518965
Exac	rs1057518965
Gnomad	rs1057518965
Varsome	rs1057518965
LitVar	rs1057518965
Map	rs1057518965
PheGenI	rs1057518965
Biobank	rs1057518965
1000 genomes	rs1057518965
hgdp	rs1057518965
ensembl	rs1057518965
geneview	rs1057518965
scholar	rs1057518965
google	rs1057518965
pharmgkb	rs1057518965
gwascentral	rs1057518965
openSNP	rs1057518965
23andMe	rs1057518965
SNPshot	rs1057518965
SNPdbe	rs1057518965
MSV3d	rs1057518965
GWAS Ctlg	rs1057518965

Max Magnitude

0

ClinVar
Risk	rs1057518965(-;-)
Alt	rs1057518965(-;-)
Reference	Rs1057518965(A;A)
Significance	Pathogenic
Disease	Ataxia Conjunctival telangiectasia Immunodeficiency Oculomotor apraxia
Variation	info
Gene	ATM
CLNDBN	Ataxia Conjunctival telangiectasia Immunodeficiency Oculomotor apraxia
Reversed	0
HGVS	NC_000011.9:g.108115539delA
CLNSRC
CLNACC	RCV000415022.1,