rs2227924

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs2227924(C;G)

Make rs2227924(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

108251865

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs2227924
dbSNP (classic)	rs2227924
ClinGen	rs2227924
ebi	rs2227924
HLI	rs2227924
Exac	rs2227924
Gnomad	rs2227924
Varsome	rs2227924
LitVar	rs2227924
Map	rs2227924
PheGenI	rs2227924
Biobank	rs2227924
1000 genomes	rs2227924
hgdp	rs2227924
ensembl	rs2227924
geneview	rs2227924
scholar	rs2227924
google	rs2227924
pharmgkb	rs2227924
gwascentral	rs2227924
openSNP	rs2227924
23andMe	rs2227924
SNPshot	rs2227924
SNPdbe	rs2227924
MSV3d	rs2227924
GWAS Ctlg	rs2227924

Merged from

Rs4987945

GMAF

0.01377

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

ClinVar
Risk	rs2227924(G;G)
Alt	rs2227924(G;G)
Reference	Rs2227924(C;C)
Significance	Other
Disease	not specified Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	ATM
CLNDBN	not specified Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108122592C>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000120117.3, RCV000128892.4, RCV000205062.4, RCV000224104.1,