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rs147557621

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147557621(A;A)
Make rs147557621(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108279510
GeneATM
is asnp
is mentioned by
dbSNPrs147557621
ebirs147557621
HLIrs147557621
Exacrs147557621
Varsomers147557621
Maprs147557621
PheGenIrs147557621
hapmaprs147557621
1000 genomesrs147557621
hgdprs147557621
ensemblrs147557621
gopubmedrs147557621
geneviewrs147557621
scholarrs147557621
googlers147557621
pharmgkbrs147557621
gwascentralrs147557621
openSNPrs147557621
23andMers147557621
23andMe allrs147557621
SNP Nexus

SNPshotrs147557621
SNPdbers147557621
MSV3drs147557621
GWAS Ctlgrs147557621
Max Magnitude0
ClinVar
Risk rs147557621(A,T;A,T)
Alt rs147557621(A,T;A,T)
Reference rs147557621(G;G)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene ATM
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108150237G>T
CLNSRC
CLNACC RCV000159714.1, RCV000213174.1,