rs587779859

Orientation

plus

Stabilized

plus

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

Make rs587779859(-;-)

Make rs587779859(-;TCTTATACAGAACAATCCCAGCCT)

Make rs587779859(TCTTATACAGAACAATCCCAGCCT;TCTTATACAGAACAATCCCAGCCT)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108327635

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587779859
dbSNP (classic)	rs587779859
ClinGen	rs587779859
ebi	rs587779859
HLI	rs587779859
Exac	rs587779859
Gnomad	rs587779859
Varsome	rs587779859
LitVar	rs587779859
Map	rs587779859
PheGenI	rs587779859
Biobank	rs587779859
1000 genomes	rs587779859
hgdp	rs587779859
ensembl	rs587779859
geneview	rs587779859
scholar	rs587779859
google	rs587779859
pharmgkb	rs587779859
gwascentral	rs587779859
openSNP	rs587779859
23andMe	rs587779859
SNPshot	rs587779859
SNPdbe	rs587779859
MSV3d	rs587779859
GWAS Ctlg	rs587779859

Max Magnitude

0

ClinVar
Risk	rs587779859(-;-)
Alt	rs587779859(-;-)
Reference	Rs587779859(TTCTTATACAGAACAATCCCAGCC;TTCTTATACAGAACAATCCCAGCC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108198362_108198385del24
CLNSRC
CLNACC	RCV000115237.2, RCV000456935.1,