rs876660813

Orientation

plus

Stabilized

plus

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

Make rs876660813(-;T)

Make rs876660813(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108353860

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876660813
dbSNP (classic)	rs876660813
ClinGen	rs876660813
ebi	rs876660813
HLI	rs876660813
Exac	rs876660813
Gnomad	rs876660813
Varsome	rs876660813
LitVar	rs876660813
Map	rs876660813
PheGenI	rs876660813
Biobank	rs876660813
1000 genomes	rs876660813
hgdp	rs876660813
ensembl	rs876660813
geneview	rs876660813
scholar	rs876660813
google	rs876660813
pharmgkb	rs876660813
gwascentral	rs876660813
openSNP	rs876660813
23andMe	rs876660813
SNPshot	rs876660813
SNPdbe	rs876660813
MSV3d	rs876660813
GWAS Ctlg	rs876660813

Max Magnitude

0

ClinVar
Risk	rs876660813(T;T)
Alt	rs876660813(T;T)
Reference	Rs876660813(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108224587dupT
CLNSRC
CLNACC	RCV000213336.1,