rs587780624

Orientation

plus

Stabilized

plus

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

Make rs587780624(-;-)

Make rs587780624(-;ATCTC)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108235815

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587780624
dbSNP (classic)	rs587780624
ClinGen	rs587780624
ebi	rs587780624
HLI	rs587780624
Exac	rs587780624
Gnomad	rs587780624
Varsome	rs587780624
LitVar	rs587780624
Map	rs587780624
PheGenI	rs587780624
Biobank	rs587780624
1000 genomes	rs587780624
hgdp	rs587780624
ensembl	rs587780624
geneview	rs587780624
scholar	rs587780624
google	rs587780624
pharmgkb	rs587780624
gwascentral	rs587780624
openSNP	rs587780624
23andMe	rs587780624
SNPshot	rs587780624
SNPdbe	rs587780624
MSV3d	rs587780624
GWAS Ctlg	rs587780624

Merged from

Rs786202225

Max Magnitude

0

ClinVar
Risk	rs587780624(-;-) rs587780624(TCTCA;TCTCA)
Alt	rs587780624(-;-) rs587780624(TCTCA;TCTCA)
Reference	Rs587780624(ATCTC;ATCTC)
Significance	Pathogenic
Disease	Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108106543_108106547delTCTCA
CLNSRC
CLNACC	RCV000122852.2, RCV000164941.3, RCV000484842.1,