rs587781730

Orientation

plus

Stabilized

plus

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

Make rs587781730(-;A)

Make rs587781730(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108307934

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587781730
dbSNP (classic)	rs587781730
ClinGen	rs587781730
ebi	rs587781730
HLI	rs587781730
Exac	rs587781730
Gnomad	rs587781730
Varsome	rs587781730
LitVar	rs587781730
Map	rs587781730
PheGenI	rs587781730
Biobank	rs587781730
1000 genomes	rs587781730
hgdp	rs587781730
ensembl	rs587781730
geneview	rs587781730
scholar	rs587781730
google	rs587781730
pharmgkb	rs587781730
gwascentral	rs587781730
openSNP	rs587781730
23andMe	rs587781730
SNPshot	rs587781730
SNPdbe	rs587781730
MSV3d	rs587781730
GWAS Ctlg	rs587781730

Max Magnitude

0

ClinVar
Risk	rs587781730(A;A)
Alt	rs587781730(A;A)
Reference	Rs587781730(-;-)
Significance	Other
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108178661dupA
CLNSRC
CLNACC	RCV000129923.6, RCV000169006.1, RCV000212031.2,