rs876658716

Orientation

plus

Stabilized

plus

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

Make rs876658716(A;A)

Make rs876658716(A;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108345873

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876658716
dbSNP (classic)	rs876658716
ClinGen	rs876658716
ebi	rs876658716
HLI	rs876658716
Exac	rs876658716
Gnomad	rs876658716
Varsome	rs876658716
LitVar	rs876658716
Map	rs876658716
PheGenI	rs876658716
Biobank	rs876658716
1000 genomes	rs876658716
hgdp	rs876658716
ensembl	rs876658716
geneview	rs876658716
scholar	rs876658716
google	rs876658716
pharmgkb	rs876658716
gwascentral	rs876658716
openSNP	rs876658716
23andMe	rs876658716
SNPshot	rs876658716
SNPdbe	rs876658716
MSV3d	rs876658716
GWAS Ctlg	rs876658716

Max Magnitude

0

ClinVar
Risk	rs876658716(A;A) rs876658716(C;C)
Alt	rs876658716(A;A) rs876658716(C;C)
Reference	Rs876658716(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000011.9:g.108216600T>A; NC_000011.9:g.108216600T>C
CLNSRC
CLNACC	RCV000215215.1, RCV000479563.1,