rs771887195

Orientation

plus

Stabilized

plus

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

Make rs771887195(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108227667

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs771887195
dbSNP (classic)	rs771887195
ClinGen	rs771887195
ebi	rs771887195
HLI	rs771887195
Exac	rs771887195
Gnomad	rs771887195
Varsome	rs771887195
LitVar	rs771887195
Map	rs771887195
PheGenI	rs771887195
Biobank	rs771887195
1000 genomes	rs771887195
hgdp	rs771887195
ensembl	rs771887195
geneview	rs771887195
scholar	rs771887195
google	rs771887195
pharmgkb	rs771887195
gwascentral	rs771887195
openSNP	rs771887195
23andMe	rs771887195
SNPshot	rs771887195
SNPdbe	rs771887195
MSV3d	rs771887195
GWAS Ctlg	rs771887195

Max Magnitude

6

ClinVar
Risk	rs771887195(-;-)
Alt	rs771887195(-;-)
Reference	Rs771887195(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108098394delC
CLNSRC
CLNACC	RCV000223089.1, RCV000481023.1,