rs772926890

Orientation

plus

Stabilized

plus

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

Make rs772926890(G;T)

Make rs772926890(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108251073

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs772926890
dbSNP (classic)	rs772926890
ClinGen	rs772926890
ebi	rs772926890
HLI	rs772926890
Exac	rs772926890
Gnomad	rs772926890
Varsome	rs772926890
LitVar	rs772926890
Map	rs772926890
PheGenI	rs772926890
Biobank	rs772926890
1000 genomes	rs772926890
hgdp	rs772926890
ensembl	rs772926890
geneview	rs772926890
scholar	rs772926890
google	rs772926890
pharmgkb	rs772926890
gwascentral	rs772926890
openSNP	rs772926890
23andMe	rs772926890
SNPshot	rs772926890
SNPdbe	rs772926890
MSV3d	rs772926890
GWAS Ctlg	rs772926890

Max Magnitude

0

ClinVar
Risk	rs772926890(T;T)
Alt	rs772926890(T;T)
Reference	Rs772926890(G;G)
Significance	Other
Disease	Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108121800G>T
CLNSRC
CLNACC	RCV000203930.1, RCV000235749.1,