rs786204726

Orientation

plus

Stabilized

plus

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

Make rs786204726(-;-)

Make rs786204726(-;ACTG)

Make rs786204726(ACTG;ACTG)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108365107

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs786204726
dbSNP (classic)	rs786204726
ClinGen	rs786204726
ebi	rs786204726
HLI	rs786204726
Exac	rs786204726
Gnomad	rs786204726
Varsome	rs786204726
LitVar	rs786204726
Map	rs786204726
PheGenI	rs786204726
Biobank	rs786204726
1000 genomes	rs786204726
hgdp	rs786204726
ensembl	rs786204726
geneview	rs786204726
scholar	rs786204726
google	rs786204726
pharmgkb	rs786204726
gwascentral	rs786204726
openSNP	rs786204726
23andMe	rs786204726
SNPshot	rs786204726
SNPdbe	rs786204726
MSV3d	rs786204726
GWAS Ctlg	rs786204726

Max Magnitude

0

ClinVar
Risk	rs786204726(-;-) Rs786204726(TGAC;TGAC)
Alt	rs786204726(-;-) Rs786204726(TGAC;TGAC)
Reference	rs786204726(ACTG;ACTG)
Significance	Other
Disease	Ataxia-telangiectasia syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Ataxia-telangiectasia syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108235834_108235837delACTG
CLNSRC
CLNACC	RCV000169561.3, RCV000236349.2, RCV000494628.1,