rs758654836

Orientation

plus

Stabilized

plus

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

Make rs758654836(C;C)

Make rs758654836(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108335958

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs758654836
dbSNP (classic)	rs758654836
ClinGen	rs758654836
ebi	rs758654836
HLI	rs758654836
Exac	rs758654836
Gnomad	rs758654836
Varsome	rs758654836
LitVar	rs758654836
Map	rs758654836
PheGenI	rs758654836
Biobank	rs758654836
1000 genomes	rs758654836
hgdp	rs758654836
ensembl	rs758654836
geneview	rs758654836
scholar	rs758654836
google	rs758654836
pharmgkb	rs758654836
gwascentral	rs758654836
openSNP	rs758654836
23andMe	rs758654836
SNPshot	rs758654836
SNPdbe	rs758654836
MSV3d	rs758654836
GWAS Ctlg	rs758654836

Max Magnitude

0

ClinVar
Risk	rs758654836(C;C) rs758654836(G;G)
Alt	rs758654836(C;C) rs758654836(G;G)
Reference	Rs758654836(T;T)
Significance	Pathogenic
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.108206685T>C; NC_000011.9:g.108206685T>G
CLNSRC
CLNACC	RCV000221847.1, RCV000472072.1, RCV000237049.1,