rs876659569

Orientation

plus

Stabilized

plus

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

Make rs876659569(-;-)

Make rs876659569(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108326100

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876659569
dbSNP (classic)	rs876659569
ClinGen	rs876659569
ebi	rs876659569
HLI	rs876659569
Exac	rs876659569
Gnomad	rs876659569
Varsome	rs876659569
LitVar	rs876659569
Map	rs876659569
PheGenI	rs876659569
Biobank	rs876659569
1000 genomes	rs876659569
hgdp	rs876659569
ensembl	rs876659569
geneview	rs876659569
scholar	rs876659569
google	rs876659569
pharmgkb	rs876659569
gwascentral	rs876659569
openSNP	rs876659569
23andMe	rs876659569
SNPshot	rs876659569
SNPdbe	rs876659569
MSV3d	rs876659569
GWAS Ctlg	rs876659569

Max Magnitude

0

ClinVar
Risk	rs876659569(-;-)
Alt	rs876659569(-;-)
Reference	Rs876659569(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108196827delG
CLNSRC
CLNACC	RCV000213820.1,