rs587781837

Orientation

plus

Stabilized

plus

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

Make rs587781837(-;-)

Make rs587781837(-;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108343350

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587781837
dbSNP (classic)	rs587781837
ClinGen	rs587781837
ebi	rs587781837
HLI	rs587781837
Exac	rs587781837
Gnomad	rs587781837
Varsome	rs587781837
LitVar	rs587781837
Map	rs587781837
PheGenI	rs587781837
Biobank	rs587781837
1000 genomes	rs587781837
hgdp	rs587781837
ensembl	rs587781837
geneview	rs587781837
scholar	rs587781837
google	rs587781837
pharmgkb	rs587781837
gwascentral	rs587781837
openSNP	rs587781837
23andMe	rs587781837
SNPshot	rs587781837
SNPdbe	rs587781837
MSV3d	rs587781837
GWAS Ctlg	rs587781837

Max Magnitude

0

ClinVar
Risk	rs587781837(-;-)
Alt	rs587781837(-;-)
Reference	Rs587781837(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108214077delT
CLNSRC
CLNACC	RCV000130132.2, RCV000255447.1,