rs786202826

Orientation

plus

Stabilized

plus

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

Make rs786202826(A;G)

Make rs786202826(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108353805

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs786202826
dbSNP (classic)	rs786202826
ClinGen	rs786202826
ebi	rs786202826
HLI	rs786202826
Exac	rs786202826
Gnomad	rs786202826
Varsome	rs786202826
LitVar	rs786202826
Map	rs786202826
PheGenI	rs786202826
Biobank	rs786202826
1000 genomes	rs786202826
hgdp	rs786202826
ensembl	rs786202826
geneview	rs786202826
scholar	rs786202826
google	rs786202826
pharmgkb	rs786202826
gwascentral	rs786202826
openSNP	rs786202826
23andMe	rs786202826
SNPshot	rs786202826
SNPdbe	rs786202826
MSV3d	rs786202826
GWAS Ctlg	rs786202826

Max Magnitude

0

ClinVar
Risk	rs786202826(G;G)
Alt	rs786202826(G;G)
Reference	Rs786202826(A;A)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108224532A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000165842.1, RCV000230822.1,