rs778031266

Orientation

plus

Stabilized

plus

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

Make rs778031266(A;A)

Make rs778031266(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108316114

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs778031266
dbSNP (classic)	rs778031266
ClinGen	rs778031266
ebi	rs778031266
HLI	rs778031266
Exac	rs778031266
Gnomad	rs778031266
Varsome	rs778031266
LitVar	rs778031266
Map	rs778031266
PheGenI	rs778031266
Biobank	rs778031266
1000 genomes	rs778031266
hgdp	rs778031266
ensembl	rs778031266
geneview	rs778031266
scholar	rs778031266
google	rs778031266
pharmgkb	rs778031266
gwascentral	rs778031266
openSNP	rs778031266
23andMe	rs778031266
SNPshot	rs778031266
SNPdbe	rs778031266
MSV3d	rs778031266
GWAS Ctlg	rs778031266

Max Magnitude

0

ClinVar
Risk	rs778031266(A;A)
Alt	rs778031266(A;A)
Reference	Rs778031266(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000011.9:g.108186841G>A
CLNSRC
CLNACC	RCV000222023.1, RCV000416815.1,