rs371638537

Orientation

plus

Stabilized

plus

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

Make rs371638537(A;T)

Make rs371638537(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

108335959

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs371638537
dbSNP (classic)	rs371638537
ClinGen	rs371638537
ebi	rs371638537
HLI	rs371638537
Exac	rs371638537
Gnomad	rs371638537
Varsome	rs371638537
LitVar	rs371638537
Map	rs371638537
PheGenI	rs371638537
Biobank	rs371638537
1000 genomes	rs371638537
hgdp	rs371638537
ensembl	rs371638537
geneview	rs371638537
scholar	rs371638537
google	rs371638537
pharmgkb	rs371638537
gwascentral	rs371638537
openSNP	rs371638537
23andMe	rs371638537
SNPshot	rs371638537
SNPdbe	rs371638537
MSV3d	rs371638537
GWAS Ctlg	rs371638537

Max Magnitude

0

ClinVar
Risk	rs371638537(C;C) rs371638537(G;G) rs371638537(T;T)
Alt	rs371638537(C;C) rs371638537(G;G) rs371638537(T;T)
Reference	Rs371638537(A;A)
Significance	Other
Disease	Hereditary cancer-predisposing syndrome not specified Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome not specified Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108206686A>C; NC_000011.9:g.108206686A>G; NC_000011.9:g.108206686A>T
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000216787.1, RCV000483443.1, RCV000122886.6, RCV000128904.5, RCV000212082.2,