rs876658832

Orientation

plus

Stabilized

plus

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

Make rs876658832(-;-)

Make rs876658832(-;TA)

Make rs876658832(TA;TA)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108247039

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876658832
dbSNP (classic)	rs876658832
ClinGen	rs876658832
ebi	rs876658832
HLI	rs876658832
Exac	rs876658832
Gnomad	rs876658832
Varsome	rs876658832
LitVar	rs876658832
Map	rs876658832
PheGenI	rs876658832
Biobank	rs876658832
1000 genomes	rs876658832
hgdp	rs876658832
ensembl	rs876658832
geneview	rs876658832
scholar	rs876658832
google	rs876658832
pharmgkb	rs876658832
gwascentral	rs876658832
openSNP	rs876658832
23andMe	rs876658832
SNPshot	rs876658832
SNPdbe	rs876658832
MSV3d	rs876658832
GWAS Ctlg	rs876658832

Max Magnitude

0

ClinVar
Risk	rs876658832(-;-)
Alt	rs876658832(-;-)
Reference	Rs876658832(AT;AT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108117766_108117767delTA
CLNSRC
CLNACC	RCV000216433.1,