rs869312755

Orientation

plus

Stabilized

plus

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

Make rs869312755(C;T)

Make rs869312755(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108293436

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs869312755
dbSNP (classic)	rs869312755
ClinGen	rs869312755
ebi	rs869312755
HLI	rs869312755
Exac	rs869312755
Gnomad	rs869312755
Varsome	rs869312755
LitVar	rs869312755
Map	rs869312755
PheGenI	rs869312755
Biobank	rs869312755
1000 genomes	rs869312755
hgdp	rs869312755
ensembl	rs869312755
geneview	rs869312755
scholar	rs869312755
google	rs869312755
pharmgkb	rs869312755
gwascentral	rs869312755
openSNP	rs869312755
23andMe	rs869312755
SNPshot	rs869312755
SNPdbe	rs869312755
MSV3d	rs869312755
GWAS Ctlg	rs869312755

Max Magnitude

0

ClinVar
Risk	rs869312755(T;T)
Alt	rs869312755(T;T)
Reference	Rs869312755(C;C)
Significance	Other
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108164163C>T
CLNSRC
CLNACC	RCV000210197.1, RCV000234068.2, RCV000255389.1,