Have questions? Visit https://www.reddit.com/r/SNPedia

rs780001540

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs780001540(A;A)
Make rs780001540(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position94459461
GeneMRE11
is asnp
is mentioned by
dbSNPrs780001540
ebirs780001540
HLIrs780001540
Exacrs780001540
Varsomers780001540
Maprs780001540
PheGenIrs780001540
hapmaprs780001540
1000 genomesrs780001540
hgdprs780001540
ensemblrs780001540
gopubmedrs780001540
geneviewrs780001540
scholarrs780001540
googlers780001540
pharmgkbrs780001540
gwascentralrs780001540
openSNPrs780001540
23andMers780001540
23andMe allrs780001540
SNP Nexus

SNPshotrs780001540
SNPdbers780001540
MSV3drs780001540
GWAS Ctlgrs780001540
Max Magnitude0
ClinVar
Risk rs780001540(A;A)
Alt rs780001540(A;A)
Reference rs780001540(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MRE11A
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.94192627G>A
CLNSRC
CLNACC RCV000216978.1,