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rs747372355

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs747372355(C;G)
Make rs747372355(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108329120
GeneATM
is asnp
is mentioned by
dbSNPrs747372355
ebirs747372355
HLIrs747372355
Exacrs747372355
Varsomers747372355
Maprs747372355
PheGenIrs747372355
hapmaprs747372355
1000 genomesrs747372355
hgdprs747372355
ensemblrs747372355
gopubmedrs747372355
geneviewrs747372355
scholarrs747372355
googlers747372355
pharmgkbrs747372355
gwascentralrs747372355
openSNPrs747372355
23andMers747372355
23andMe allrs747372355
SNP Nexus

SNPshotrs747372355
SNPdbers747372355
MSV3drs747372355
GWAS Ctlgrs747372355
Max Magnitude0
ClinVar
Risk rs747372355(G;G)
Alt rs747372355(G;G)
Reference rs747372355(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108199847C>T
CLNSRC
CLNACC RCV000219784.1,