rs876659365

Orientation

plus

Stabilized

plus

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

Make rs876659365(G;G)

Make rs876659365(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108330314

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876659365
dbSNP (classic)	rs876659365
ClinGen	rs876659365
ebi	rs876659365
HLI	rs876659365
Exac	rs876659365
Gnomad	rs876659365
Varsome	rs876659365
LitVar	rs876659365
Map	rs876659365
PheGenI	rs876659365
Biobank	rs876659365
1000 genomes	rs876659365
hgdp	rs876659365
ensembl	rs876659365
geneview	rs876659365
scholar	rs876659365
google	rs876659365
pharmgkb	rs876659365
gwascentral	rs876659365
openSNP	rs876659365
23andMe	rs876659365
SNPshot	rs876659365
SNPdbe	rs876659365
MSV3d	rs876659365
GWAS Ctlg	rs876659365

Max Magnitude

0

ClinVar
Risk	rs876659365(G;G)
Alt	rs876659365(G;G)
Reference	Rs876659365(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108201041T>G
CLNSRC
CLNACC	RCV000220077.1,