rs876659535

Orientation

plus

Stabilized

plus

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

Make rs876659535(-;-)

Make rs876659535(-;GATA)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108293343

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876659535
dbSNP (classic)	rs876659535
ClinGen	rs876659535
ebi	rs876659535
HLI	rs876659535
Exac	rs876659535
Gnomad	rs876659535
Varsome	rs876659535
LitVar	rs876659535
Map	rs876659535
PheGenI	rs876659535
Biobank	rs876659535
1000 genomes	rs876659535
hgdp	rs876659535
ensembl	rs876659535
geneview	rs876659535
scholar	rs876659535
google	rs876659535
pharmgkb	rs876659535
gwascentral	rs876659535
openSNP	rs876659535
23andMe	rs876659535
SNPshot	rs876659535
SNPdbe	rs876659535
MSV3d	rs876659535
GWAS Ctlg	rs876659535

Max Magnitude

0

ClinVar
Risk	rs876659535(-;-)
Alt	rs876659535(-;-)
Reference	Rs876659535(GATA;GATA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108164070_108164073delGATA
CLNSRC
CLNACC	RCV000214019.1,