rs121434222

Orientation

plus

Stabilized

plus

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

Make rs121434222(C;T)

Make rs121434222(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

108287687

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs121434222
dbSNP (classic)	rs121434222
ClinGen	rs121434222
ebi	rs121434222
HLI	rs121434222
Exac	rs121434222
Gnomad	rs121434222
Varsome	rs121434222
LitVar	rs121434222
Map	rs121434222
PheGenI	rs121434222
Biobank	rs121434222
1000 genomes	rs121434222
hgdp	rs121434222
ensembl	rs121434222
geneview	rs121434222
scholar	rs121434222
google	rs121434222
pharmgkb	rs121434222
gwascentral	rs121434222
openSNP	rs121434222
23andMe	rs121434222
SNPshot	rs121434222
SNPdbe	rs121434222
MSV3d	rs121434222
GWAS Ctlg	rs121434222

Max Magnitude

0

OMIM	607585
Desc
Variant	0024
Related	also

ClinVar
Risk	rs121434222(T;T)
Alt	rs121434222(T;T)
Reference	Rs121434222(C;C)
Significance	Pathogenic
Disease	Mantle cell lymphoma
Variation	info
Gene	ATM
CLNDBN	Mantle cell lymphoma
Reversed	0
HGVS	NC_000011.9:g.108158414C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003182.7,