rs730881299

Orientation

plus

Stabilized

plus

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

Make rs730881299(-;T)

Make rs730881299(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108267268

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs730881299
dbSNP (classic)	rs730881299
ClinGen	rs730881299
ebi	rs730881299
HLI	rs730881299
Exac	rs730881299
Gnomad	rs730881299
Varsome	rs730881299
LitVar	rs730881299
Map	rs730881299
PheGenI	rs730881299
Biobank	rs730881299
1000 genomes	rs730881299
hgdp	rs730881299
ensembl	rs730881299
geneview	rs730881299
scholar	rs730881299
google	rs730881299
pharmgkb	rs730881299
gwascentral	rs730881299
openSNP	rs730881299
23andMe	rs730881299
SNPshot	rs730881299
SNPdbe	rs730881299
MSV3d	rs730881299
GWAS Ctlg	rs730881299

Max Magnitude

0

ClinVar
Risk	rs730881299(T;T)
Alt	rs730881299(T;T)
Reference	Rs730881299(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108137995dupT
CLNSRC
CLNACC	RCV000159628.1,