rs786203817

Orientation

plus

Stabilized

plus

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

Make rs786203817(-;-)

Make rs786203817(-;TT)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108282759

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs786203817
dbSNP (classic)	rs786203817
ClinGen	rs786203817
ebi	rs786203817
HLI	rs786203817
Exac	rs786203817
Gnomad	rs786203817
Varsome	rs786203817
LitVar	rs786203817
Map	rs786203817
PheGenI	rs786203817
Biobank	rs786203817
1000 genomes	rs786203817
hgdp	rs786203817
ensembl	rs786203817
geneview	rs786203817
scholar	rs786203817
google	rs786203817
pharmgkb	rs786203817
gwascentral	rs786203817
openSNP	rs786203817
23andMe	rs786203817
SNPshot	rs786203817
SNPdbe	rs786203817
MSV3d	rs786203817
GWAS Ctlg	rs786203817

Max Magnitude

0

ClinVar
Risk	rs786203817(-;-)
Alt	rs786203817(-;-)
Reference	Rs786203817(TT;TT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108153486_108153487delTT
CLNSRC
CLNACC	RCV000167290.2, RCV000235460.1,