rs876659866

Orientation

plus

Stabilized

plus

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

Make rs876659866(-;-)

Make rs876659866(-;GT)

Make rs876659866(GT;GT)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108250859

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876659866
dbSNP (classic)	rs876659866
ClinGen	rs876659866
ebi	rs876659866
HLI	rs876659866
Exac	rs876659866
Gnomad	rs876659866
Varsome	rs876659866
LitVar	rs876659866
Map	rs876659866
PheGenI	rs876659866
Biobank	rs876659866
1000 genomes	rs876659866
hgdp	rs876659866
ensembl	rs876659866
geneview	rs876659866
scholar	rs876659866
google	rs876659866
pharmgkb	rs876659866
gwascentral	rs876659866
openSNP	rs876659866
23andMe	rs876659866
SNPshot	rs876659866
SNPdbe	rs876659866
MSV3d	rs876659866
GWAS Ctlg	rs876659866

Max Magnitude

0

ClinVar
Risk	rs876659866(-;-)
Alt	rs876659866(-;-)
Reference	Rs876659866(TG;TG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108121586_108121587delGT
CLNSRC
CLNACC	RCV000216302.1,