rs876660041

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(TAATG;TAATG)	0	common in clinvar
(TGTAA;TGTAA)	0	common in clinvar

Make rs876660041(-;-)

Make rs876660041(-;TGTAA)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108331557

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876660041
dbSNP (classic)	rs876660041
ClinGen	rs876660041
ebi	rs876660041
HLI	rs876660041
Exac	rs876660041
Gnomad	rs876660041
Varsome	rs876660041
LitVar	rs876660041
Map	rs876660041
PheGenI	rs876660041
Biobank	rs876660041
1000 genomes	rs876660041
hgdp	rs876660041
ensembl	rs876660041
geneview	rs876660041
scholar	rs876660041
google	rs876660041
pharmgkb	rs876660041
gwascentral	rs876660041
openSNP	rs876660041
23andMe	rs876660041
SNPshot	rs876660041
SNPdbe	rs876660041
MSV3d	rs876660041
GWAS Ctlg	rs876660041

Max Magnitude

0

ClinVar
Risk	rs876660041(-;-) Rs876660041(TAATG;TAATG)
Alt	rs876660041(-;-) Rs876660041(TAATG;TAATG)
Reference	Rs876660041(TGTAA;TGTAA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108202284_108202288delTGTAA
CLNSRC
CLNACC	RCV000219911.1, RCV000476426.1,