rs876660411

Orientation

plus

Stabilized

plus

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

Make rs876660411(-;A)

Make rs876660411(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108347318

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876660411
dbSNP (classic)	rs876660411
ClinGen	rs876660411
ebi	rs876660411
HLI	rs876660411
Exac	rs876660411
Gnomad	rs876660411
Varsome	rs876660411
LitVar	rs876660411
Map	rs876660411
PheGenI	rs876660411
Biobank	rs876660411
1000 genomes	rs876660411
hgdp	rs876660411
ensembl	rs876660411
geneview	rs876660411
scholar	rs876660411
google	rs876660411
pharmgkb	rs876660411
gwascentral	rs876660411
openSNP	rs876660411
23andMe	rs876660411
SNPshot	rs876660411
SNPdbe	rs876660411
MSV3d	rs876660411
GWAS Ctlg	rs876660411

Max Magnitude

0

ClinVar
Risk	rs876660411(A;A)
Alt	rs876660411(A;A)
Reference	Rs876660411(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108218045dupA
CLNSRC
CLNACC	RCV000223413.1,