rs1057517097

Orientation

plus

Stabilized

plus

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

Make rs1057517097(-;T)

Make rs1057517097(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108272799

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs1057517097
dbSNP (classic)	rs1057517097
ClinGen	rs1057517097
ebi	rs1057517097
HLI	rs1057517097
Exac	rs1057517097
Gnomad	rs1057517097
Varsome	rs1057517097
LitVar	rs1057517097
Map	rs1057517097
PheGenI	rs1057517097
Biobank	rs1057517097
1000 genomes	rs1057517097
hgdp	rs1057517097
ensembl	rs1057517097
geneview	rs1057517097
scholar	rs1057517097
google	rs1057517097
pharmgkb	rs1057517097
gwascentral	rs1057517097
openSNP	rs1057517097
23andMe	rs1057517097
SNPshot	rs1057517097
SNPdbe	rs1057517097
MSV3d	rs1057517097
GWAS Ctlg	rs1057517097

Max Magnitude

0

ClinVar
Risk	rs1057517097(T;T)
Alt	rs1057517097(T;T)
Reference	Rs1057517097(-;-)
Significance	Probable-Pathogenic
Disease	Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108143526dupT
CLNSRC
CLNACC	RCV000409693.1,