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rs876660061

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660061(-;-)
Make rs876660061(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214780851
GeneBARD1
is asnp
is mentioned by
dbSNPrs876660061
ebirs876660061
HLIrs876660061
Exacrs876660061
Varsomers876660061
Maprs876660061
PheGenIrs876660061
hapmaprs876660061
1000 genomesrs876660061
hgdprs876660061
ensemblrs876660061
gopubmedrs876660061
geneviewrs876660061
scholarrs876660061
googlers876660061
pharmgkbrs876660061
gwascentralrs876660061
openSNPrs876660061
23andMers876660061
23andMe allrs876660061
SNP Nexus

SNPshotrs876660061
SNPdbers876660061
MSV3drs876660061
GWAS Ctlgrs876660061
Max Magnitude0
ClinVar
Risk rs876660061(;)
Alt rs876660061(;)
Reference rs876660061(G;G)
Significance 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.215645575delC
CLNSRC
CLNACC RCV000215348.1,