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rs876659450

From SNPedia

Orientationplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs876659450(-;-)
Make rs876659450(-;GG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108249046
GeneATM
is asnp
is mentioned by
dbSNPrs876659450
ebirs876659450
HLIrs876659450
Exacrs876659450
Varsomers876659450
Maprs876659450
PheGenIrs876659450
hapmaprs876659450
1000 genomesrs876659450
hgdprs876659450
ensemblrs876659450
gopubmedrs876659450
geneviewrs876659450
scholarrs876659450
googlers876659450
pharmgkbrs876659450
gwascentralrs876659450
openSNPrs876659450
23andMers876659450
23andMe allrs876659450
SNP Nexus

SNPshotrs876659450
SNPdbers876659450
MSV3drs876659450
GWAS Ctlgrs876659450
Max Magnitude0
ClinVar
Risk rs876659450(;)
Alt rs876659450(;)
Reference rs876659450(GG;GG)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108119773_108119774delGG
CLNSRC
CLNACC RCV000219422.1,