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rs876659560

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659560(-;-)
Make rs876659560(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214730510
GeneBARD1
is asnp
is mentioned by
dbSNPrs876659560
ebirs876659560
HLIrs876659560
Exacrs876659560
Varsomers876659560
Maprs876659560
PheGenIrs876659560
hapmaprs876659560
1000 genomesrs876659560
hgdprs876659560
ensemblrs876659560
gopubmedrs876659560
geneviewrs876659560
scholarrs876659560
googlers876659560
pharmgkbrs876659560
gwascentralrs876659560
openSNPrs876659560
23andMers876659560
23andMe allrs876659560
SNP Nexus

SNPshotrs876659560
SNPdbers876659560
MSV3drs876659560
GWAS Ctlgrs876659560
Max Magnitude0
ClinVar
Risk rs876659560(;)
Alt rs876659560(;)
Reference rs876659560(A;A)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BARD1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000002.11:g.215595234delT
CLNSRC
CLNACC RCV000217479.1,