rs876660933

Orientation

plus

Stabilized

plus

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

Make rs876660933(G;T)

Make rs876660933(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108244954

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876660933
dbSNP (classic)	rs876660933
ClinGen	rs876660933
ebi	rs876660933
HLI	rs876660933
Exac	rs876660933
Gnomad	rs876660933
Varsome	rs876660933
LitVar	rs876660933
Map	rs876660933
PheGenI	rs876660933
Biobank	rs876660933
1000 genomes	rs876660933
hgdp	rs876660933
ensembl	rs876660933
geneview	rs876660933
scholar	rs876660933
google	rs876660933
pharmgkb	rs876660933
gwascentral	rs876660933
openSNP	rs876660933
23andMe	rs876660933
SNPshot	rs876660933
SNPdbe	rs876660933
MSV3d	rs876660933
GWAS Ctlg	rs876660933

Max Magnitude

0

ClinVar
Risk	rs876660933(T;T)
Alt	rs876660933(T;T)
Reference	Rs876660933(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108115681G>T
CLNSRC
CLNACC	RCV000223320.1, RCV000235851.1,