rs1057516833

Orientation

plus

Stabilized

plus

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

Make rs1057516833(C;G)

Make rs1057516833(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108329097

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs1057516833
dbSNP (classic)	rs1057516833
ClinGen	rs1057516833
ebi	rs1057516833
HLI	rs1057516833
Exac	rs1057516833
Gnomad	rs1057516833
Varsome	rs1057516833
LitVar	rs1057516833
Map	rs1057516833
PheGenI	rs1057516833
Biobank	rs1057516833
1000 genomes	rs1057516833
hgdp	rs1057516833
ensembl	rs1057516833
geneview	rs1057516833
scholar	rs1057516833
google	rs1057516833
pharmgkb	rs1057516833
gwascentral	rs1057516833
openSNP	rs1057516833
23andMe	rs1057516833
SNPshot	rs1057516833
SNPdbe	rs1057516833
MSV3d	rs1057516833
GWAS Ctlg	rs1057516833

Max Magnitude

0

ClinVar
Risk	rs1057516833(G;G) rs1057516833(T;T)
Alt	rs1057516833(G;G) rs1057516833(T;T)
Reference	Rs1057516833(C;C)
Significance	Probable-Pathogenic
Disease	Ataxia-telangiectasia syndrome not specified
Variation	info
Gene	C11orf65 ATM
CLNDBN	Ataxia-telangiectasia syndrome not specified
Reversed	0
HGVS	NC_000011.9:g.108199824C>G; NC_000011.9:g.108199824C>T
CLNSRC
CLNACC	RCV000411247.1, RCV000436625.1,