rs730881362

Orientation

plus

Stabilized

plus

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

Make rs730881362(G;T)

Make rs730881362(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108227857

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs730881362
dbSNP (classic)	rs730881362
ClinGen	rs730881362
ebi	rs730881362
HLI	rs730881362
Exac	rs730881362
Gnomad	rs730881362
Varsome	rs730881362
LitVar	rs730881362
Map	rs730881362
PheGenI	rs730881362
Biobank	rs730881362
1000 genomes	rs730881362
hgdp	rs730881362
ensembl	rs730881362
geneview	rs730881362
scholar	rs730881362
google	rs730881362
pharmgkb	rs730881362
gwascentral	rs730881362
openSNP	rs730881362
23andMe	rs730881362
SNPshot	rs730881362
SNPdbe	rs730881362
MSV3d	rs730881362
GWAS Ctlg	rs730881362

Max Magnitude

0

ClinVar
Risk	rs730881362(T;T)
Alt	rs730881362(T;T)
Reference	Rs730881362(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ATM
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.108098584G>T
CLNSRC
CLNACC	RCV000159713.2,