rs587782525

Orientation

plus

Stabilized

plus

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

Make rs587782525(-;AA)

Make rs587782525(AA;AA)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108335898

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587782525
dbSNP (classic)	rs587782525
ClinGen	rs587782525
ebi	rs587782525
HLI	rs587782525
Exac	rs587782525
Gnomad	rs587782525
Varsome	rs587782525
LitVar	rs587782525
Map	rs587782525
PheGenI	rs587782525
Biobank	rs587782525
1000 genomes	rs587782525
hgdp	rs587782525
ensembl	rs587782525
geneview	rs587782525
scholar	rs587782525
google	rs587782525
pharmgkb	rs587782525
gwascentral	rs587782525
openSNP	rs587782525
23andMe	rs587782525
SNPshot	rs587782525
SNPdbe	rs587782525
MSV3d	rs587782525
GWAS Ctlg	rs587782525

Max Magnitude

0

ClinVar
Risk	rs587782525(AA;AA) rs587782525(GT;GT)
Alt	rs587782525(AA;AA) rs587782525(GT;GT)
Reference	Rs587782525(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108206624_108206625dupGT; NC_000011.9:g.108206625_108206626insAA
CLNSRC
CLNACC	RCV000215590.1, RCV000131713.2,