rs786203606

Orientation

plus

Stabilized

plus

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

Make rs786203606(C;C)

Make rs786203606(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108227626

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs786203606
dbSNP (classic)	rs786203606
ClinGen	rs786203606
ebi	rs786203606
HLI	rs786203606
Exac	rs786203606
Gnomad	rs786203606
Varsome	rs786203606
LitVar	rs786203606
Map	rs786203606
PheGenI	rs786203606
Biobank	rs786203606
1000 genomes	rs786203606
hgdp	rs786203606
ensembl	rs786203606
geneview	rs786203606
scholar	rs786203606
google	rs786203606
pharmgkb	rs786203606
gwascentral	rs786203606
openSNP	rs786203606
23andMe	rs786203606
SNPshot	rs786203606
SNPdbe	rs786203606
MSV3d	rs786203606
GWAS Ctlg	rs786203606

Max Magnitude

0

ClinVar
Risk	rs786203606(C;C)
Alt	rs786203606(C;C)
Reference	Rs786203606(T;T)
Significance	Other
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108098353T>C
CLNSRC
CLNACC	RCV000166992.2, RCV000168377.6,