rs587782847

Orientation

plus

Stabilized

plus

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

Make rs587782847(-;-)

Make rs587782847(-;AACTGAAAGGA)

Make rs587782847(AACTGAAAGGA;AACTGAAAGGA)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108365384

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587782847
dbSNP (classic)	rs587782847
ClinGen	rs587782847
ebi	rs587782847
HLI	rs587782847
Exac	rs587782847
Gnomad	rs587782847
Varsome	rs587782847
LitVar	rs587782847
Map	rs587782847
PheGenI	rs587782847
Biobank	rs587782847
1000 genomes	rs587782847
hgdp	rs587782847
ensembl	rs587782847
geneview	rs587782847
scholar	rs587782847
google	rs587782847
pharmgkb	rs587782847
gwascentral	rs587782847
openSNP	rs587782847
23andMe	rs587782847
SNPshot	rs587782847
SNPdbe	rs587782847
MSV3d	rs587782847
GWAS Ctlg	rs587782847

Max Magnitude

0

ClinVar
Risk	rs587782847(-;-)
Alt	rs587782847(-;-)
Reference	Rs587782847(GAAACTGAAAG;GAAACTGAAAG)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108236111_108236121delAACTGAAAGGA
CLNSRC
CLNACC	RCV000132441.2,