rs876659672

Orientation

plus

Stabilized

plus

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

Make rs876659672(-;G)

Make rs876659672(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108284415

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876659672
dbSNP (classic)	rs876659672
ClinGen	rs876659672
ebi	rs876659672
HLI	rs876659672
Exac	rs876659672
Gnomad	rs876659672
Varsome	rs876659672
LitVar	rs876659672
Map	rs876659672
PheGenI	rs876659672
Biobank	rs876659672
1000 genomes	rs876659672
hgdp	rs876659672
ensembl	rs876659672
geneview	rs876659672
scholar	rs876659672
google	rs876659672
pharmgkb	rs876659672
gwascentral	rs876659672
openSNP	rs876659672
23andMe	rs876659672
SNPshot	rs876659672
SNPdbe	rs876659672
MSV3d	rs876659672
GWAS Ctlg	rs876659672

Max Magnitude

0

ClinVar
Risk	rs876659672(G;G)
Alt	rs876659672(G;G)
Reference	Rs876659672(-;-)
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.108155142dupG
CLNSRC
CLNACC	RCV000223199.1, RCV000411978.1, RCV000483621.1,