rs139770721

Orientation

plus

Stabilized

plus

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

Make rs139770721(A;A)

Make rs139770721(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108315911

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs139770721
dbSNP (classic)	rs139770721
ClinGen	rs139770721
ebi	rs139770721
HLI	rs139770721
Exac	rs139770721
Gnomad	rs139770721
Varsome	rs139770721
LitVar	rs139770721
Map	rs139770721
PheGenI	rs139770721
Biobank	rs139770721
1000 genomes	rs139770721
hgdp	rs139770721
ensembl	rs139770721
geneview	rs139770721
scholar	rs139770721
google	rs139770721
pharmgkb	rs139770721
gwascentral	rs139770721
openSNP	rs139770721
23andMe	rs139770721
SNPshot	rs139770721
SNPdbe	rs139770721
MSV3d	rs139770721
GWAS Ctlg	rs139770721

Max Magnitude

0

ClinVar
Risk	rs139770721(A;A)
Alt	rs139770721(A;A)
Reference	Rs139770721(G;G)
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.108186638G>A
CLNSRC
CLNACC	RCV000159742.5, RCV000167946.4, RCV000212037.2,