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rs796051857

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796051857(-;GAA)
Make rs796051857(GAA;GAA)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108329184
GeneATM
is asnp
is mentioned by
dbSNPrs796051857
ClinGenrs796051857
ebirs796051857
HLIrs796051857
Exacrs796051857
Varsomers796051857
Maprs796051857
PheGenIrs796051857
hapmaprs796051857
1000 genomesrs796051857
hgdprs796051857
ensemblrs796051857
gopubmedrs796051857
geneviewrs796051857
scholarrs796051857
googlers796051857
pharmgkbrs796051857
gwascentralrs796051857
openSNPrs796051857
23andMers796051857
23andMe allrs796051857
SNP Nexus

SNPshotrs796051857
SNPdbers796051857
MSV3drs796051857
GWAS Ctlgrs796051857
Max Magnitude0
ClinVar
Risk rs796051857(GAA;GAA)
Alt rs796051857(GAA;GAA)
Reference Rs796051857(;)
Significance Pathogenic
Disease Mantle cell lymphoma
Variation info
Gene C11orf65 ATM
CLNDBN Mantle cell lymphoma
Reversed 0
HGVS NC_000011.9:g.108199909_108199911dupGAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000003181.4,