rs764389018

Orientation

plus

Stabilized

plus

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

Make rs764389018(C;T)

Make rs764389018(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108301658

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs764389018
dbSNP (classic)	rs764389018
ClinGen	rs764389018
ebi	rs764389018
HLI	rs764389018
Exac	rs764389018
Gnomad	rs764389018
Varsome	rs764389018
LitVar	rs764389018
Map	rs764389018
PheGenI	rs764389018
Biobank	rs764389018
1000 genomes	rs764389018
hgdp	rs764389018
ensembl	rs764389018
geneview	rs764389018
scholar	rs764389018
google	rs764389018
pharmgkb	rs764389018
gwascentral	rs764389018
openSNP	rs764389018
23andMe	rs764389018
SNPshot	rs764389018
SNPdbe	rs764389018
MSV3d	rs764389018
GWAS Ctlg	rs764389018

Max Magnitude

0

ClinVar
Risk	rs764389018(T;T)
Alt	rs764389018(T;T)
Reference	Rs764389018(C;C)
Significance	Other
Disease	Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108172385C>T
CLNSRC
CLNACC	RCV000169451.2,