rs876660315

Orientation

plus

Stabilized

plus

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

Make rs876660315(-;-)

Make rs876660315(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108244098

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876660315
dbSNP (classic)	rs876660315
ClinGen	rs876660315
ebi	rs876660315
HLI	rs876660315
Exac	rs876660315
Gnomad	rs876660315
Varsome	rs876660315
LitVar	rs876660315
Map	rs876660315
PheGenI	rs876660315
Biobank	rs876660315
1000 genomes	rs876660315
hgdp	rs876660315
ensembl	rs876660315
geneview	rs876660315
scholar	rs876660315
google	rs876660315
pharmgkb	rs876660315
gwascentral	rs876660315
openSNP	rs876660315
23andMe	rs876660315
SNPshot	rs876660315
SNPdbe	rs876660315
MSV3d	rs876660315
GWAS Ctlg	rs876660315

Max Magnitude

0

ClinVar
Risk	rs876660315(-;-)
Alt	rs876660315(-;-)
Reference	Rs876660315(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108114825delC
CLNSRC
CLNACC	RCV000219456.1,