rs876659010

Orientation

plus

Stabilized

plus

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

Make rs876659010(-;A)

Make rs876659010(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108345838

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876659010
dbSNP (classic)	rs876659010
ClinGen	rs876659010
ebi	rs876659010
HLI	rs876659010
Exac	rs876659010
Gnomad	rs876659010
Varsome	rs876659010
LitVar	rs876659010
Map	rs876659010
PheGenI	rs876659010
Biobank	rs876659010
1000 genomes	rs876659010
hgdp	rs876659010
ensembl	rs876659010
geneview	rs876659010
scholar	rs876659010
google	rs876659010
pharmgkb	rs876659010
gwascentral	rs876659010
openSNP	rs876659010
23andMe	rs876659010
SNPshot	rs876659010
SNPdbe	rs876659010
MSV3d	rs876659010
GWAS Ctlg	rs876659010

Max Magnitude

0

ClinVar
Risk	rs876659010(A;A)
Alt	rs876659010(A;A)
Reference	Rs876659010(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108216565dupA
CLNSRC
CLNACC	RCV000221706.1,