rs786202087

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	6	Breast cancer associated mutation

Make rs786202087(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108365323

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs786202087
dbSNP (classic)	rs786202087
ClinGen	rs786202087
ebi	rs786202087
HLI	rs786202087
Exac	rs786202087
Gnomad	rs786202087
Varsome	rs786202087
LitVar	rs786202087
Map	rs786202087
PheGenI	rs786202087
Biobank	rs786202087
1000 genomes	rs786202087
hgdp	rs786202087
ensembl	rs786202087
geneview	rs786202087
scholar	rs786202087
google	rs786202087
pharmgkb	rs786202087
gwascentral	rs786202087
openSNP	rs786202087
23andMe	rs786202087
SNPshot	rs786202087
SNPdbe	rs786202087
MSV3d	rs786202087
GWAS Ctlg	rs786202087

Max Magnitude

6

ClinVar
Risk	rs786202087(G;G)
Alt	rs786202087(G;G)
Reference	Rs786202087(A;A)
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.108236050A>G
CLNSRC
CLNACC	RCV000164726.2,