rs1057517226

Orientation

plus

Stabilized

plus

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

Make rs1057517226(C;C)

Make rs1057517226(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108282709

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs1057517226
dbSNP (classic)	rs1057517226
ClinGen	rs1057517226
ebi	rs1057517226
HLI	rs1057517226
Exac	rs1057517226
Gnomad	rs1057517226
Varsome	rs1057517226
LitVar	rs1057517226
Map	rs1057517226
PheGenI	rs1057517226
Biobank	rs1057517226
1000 genomes	rs1057517226
hgdp	rs1057517226
ensembl	rs1057517226
geneview	rs1057517226
scholar	rs1057517226
google	rs1057517226
pharmgkb	rs1057517226
gwascentral	rs1057517226
openSNP	rs1057517226
23andMe	rs1057517226
SNPshot	rs1057517226
SNPdbe	rs1057517226
MSV3d	rs1057517226
GWAS Ctlg	rs1057517226

Max Magnitude

0

ClinVar
Risk	rs1057517226(C;C)
Alt	rs1057517226(C;C)
Reference	Rs1057517226(G;G)
Significance	Probable-Pathogenic
Disease	Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108153436G>C
CLNSRC
CLNACC	RCV000410163.1,