rs886039623

Orientation

plus

Stabilized

plus

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

Make rs886039623(-;-)

Make rs886039623(-;C)

Reference

GRCh38.p7 38.3/149

Chromosome

11

Position

108343278

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs886039623
dbSNP (classic)	rs886039623
ClinGen	rs886039623
ebi	rs886039623
HLI	rs886039623
Exac	rs886039623
Gnomad	rs886039623
Varsome	rs886039623
LitVar	rs886039623
Map	rs886039623
PheGenI	rs886039623
Biobank	rs886039623
1000 genomes	rs886039623
hgdp	rs886039623
ensembl	rs886039623
geneview	rs886039623
scholar	rs886039623
google	rs886039623
pharmgkb	rs886039623
gwascentral	rs886039623
openSNP	rs886039623
23andMe	rs886039623
SNPshot	rs886039623
SNPdbe	rs886039623
MSV3d	rs886039623
GWAS Ctlg	rs886039623

Max Magnitude

0

ClinVar
Risk	rs886039623(-;-)
Alt	rs886039623(-;-)
Reference	Rs886039623(C;C)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108214005delC
CLNSRC
CLNACC	RCV000255611.1, RCV000494589.1,