rs1137887

Orientation

plus

Stabilized

plus

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

Make rs1137887(A;A)

Make rs1137887(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108256340

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs1137887
dbSNP (classic)	rs1137887
ClinGen	rs1137887
ebi	rs1137887
HLI	rs1137887
Exac	rs1137887
Gnomad	rs1137887
Varsome	rs1137887
LitVar	rs1137887
Map	rs1137887
PheGenI	rs1137887
Biobank	rs1137887
1000 genomes	rs1137887
hgdp	rs1137887
ensembl	rs1137887
geneview	rs1137887
scholar	rs1137887
google	rs1137887
pharmgkb	rs1137887
gwascentral	rs1137887
openSNP	rs1137887
23andMe	rs1137887
SNPshot	rs1137887
SNPdbe	rs1137887
MSV3d	rs1137887
GWAS Ctlg	rs1137887

Max Magnitude

0

ClinVar
Risk	rs1137887(A;A)
Alt	rs1137887(A;A)
Reference	Rs1137887(G;G)
Significance	Other
Disease	Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108127067G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003185.9, RCV000115149.9, RCV000235101.1,