rs786204737

Orientation

plus

Stabilized

plus

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

Make rs786204737(-;-)

Make rs786204737(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108250989

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs786204737
dbSNP (classic)	rs786204737
ClinGen	rs786204737
ebi	rs786204737
HLI	rs786204737
Exac	rs786204737
Gnomad	rs786204737
Varsome	rs786204737
LitVar	rs786204737
Map	rs786204737
PheGenI	rs786204737
Biobank	rs786204737
1000 genomes	rs786204737
hgdp	rs786204737
ensembl	rs786204737
geneview	rs786204737
scholar	rs786204737
google	rs786204737
pharmgkb	rs786204737
gwascentral	rs786204737
openSNP	rs786204737
23andMe	rs786204737
SNPshot	rs786204737
SNPdbe	rs786204737
MSV3d	rs786204737
GWAS Ctlg	rs786204737

Max Magnitude

0

ClinVar
Risk	rs786204737(-;-)
Alt	rs786204737(-;-)
Reference	Rs786204737(T;T)
Significance	Probable-Pathogenic
Disease	Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108121716delT
CLNSRC
CLNACC	RCV000169584.1, RCV000236634.1,