rs876658182

Orientation

plus

Stabilized

plus

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

Make rs876658182(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108345909

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876658182
dbSNP (classic)	rs876658182
ClinGen	rs876658182
ebi	rs876658182
HLI	rs876658182
Exac	rs876658182
Gnomad	rs876658182
Varsome	rs876658182
LitVar	rs876658182
Map	rs876658182
PheGenI	rs876658182
Biobank	rs876658182
1000 genomes	rs876658182
hgdp	rs876658182
ensembl	rs876658182
geneview	rs876658182
scholar	rs876658182
google	rs876658182
pharmgkb	rs876658182
gwascentral	rs876658182
openSNP	rs876658182
23andMe	rs876658182
SNPshot	rs876658182
SNPdbe	rs876658182
MSV3d	rs876658182
GWAS Ctlg	rs876658182

Max Magnitude

6

ClinVar
Risk	rs876658182(A;A)
Alt	rs876658182(A;A)
Reference	Rs876658182(G;G)
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.108216636G>A
CLNSRC
CLNACC	RCV000213099.2,