rs786202264

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GAAAGTCTCAAAT)	6	Breast cancer associated mutation
(ATGAAAGTCTCAA;ATGAAAGTCTCAA)	0	common in clinvar

Make rs786202264(-;-)

Make rs786202264(GAAAGTCTCAAAT;GAAAGTCTCAAAT)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108320039

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs786202264
dbSNP (classic)	rs786202264
ClinGen	rs786202264
ebi	rs786202264
HLI	rs786202264
Exac	rs786202264
Gnomad	rs786202264
Varsome	rs786202264
LitVar	rs786202264
Map	rs786202264
PheGenI	rs786202264
Biobank	rs786202264
1000 genomes	rs786202264
hgdp	rs786202264
ensembl	rs786202264
geneview	rs786202264
scholar	rs786202264
google	rs786202264
pharmgkb	rs786202264
gwascentral	rs786202264
openSNP	rs786202264
23andMe	rs786202264
SNPshot	rs786202264
SNPdbe	rs786202264
MSV3d	rs786202264
GWAS Ctlg	rs786202264

Max Magnitude

6

ClinVar
Risk	rs786202264(-;-)
Alt	rs786202264(-;-)
Reference	Rs786202264(ATGAAAGTCTCAA;ATGAAAGTCTCAA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108190766_108190778delGAAAGTCTCAAAT
CLNSRC
CLNACC	RCV000164992.1,