rs876659450

Orientation

plus

Stabilized

plus

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

Make rs876659450(-;-)

Make rs876659450(-;GG)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108249046

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876659450
dbSNP (classic)	rs876659450
ClinGen	rs876659450
ebi	rs876659450
HLI	rs876659450
Exac	rs876659450
Gnomad	rs876659450
Varsome	rs876659450
LitVar	rs876659450
Map	rs876659450
PheGenI	rs876659450
Biobank	rs876659450
1000 genomes	rs876659450
hgdp	rs876659450
ensembl	rs876659450
geneview	rs876659450
scholar	rs876659450
google	rs876659450
pharmgkb	rs876659450
gwascentral	rs876659450
openSNP	rs876659450
23andMe	rs876659450
SNPshot	rs876659450
SNPdbe	rs876659450
MSV3d	rs876659450
GWAS Ctlg	rs876659450

Max Magnitude

0

ClinVar
Risk	rs876659450(-;-)
Alt	rs876659450(-;-)
Reference	Rs876659450(GG;GG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108119773_108119774delGG
CLNSRC
CLNACC	RCV000219422.1, RCV000479095.1,