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rs876658571

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658571(C;T)
Make rs876658571(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214792384
GeneBARD1
is asnp
is mentioned by
dbSNPrs876658571
ebirs876658571
HLIrs876658571
Exacrs876658571
Varsomers876658571
Maprs876658571
PheGenIrs876658571
hapmaprs876658571
1000 genomesrs876658571
hgdprs876658571
ensemblrs876658571
gopubmedrs876658571
geneviewrs876658571
scholarrs876658571
googlers876658571
pharmgkbrs876658571
gwascentralrs876658571
openSNPrs876658571
23andMers876658571
23andMe allrs876658571
SNP Nexus

SNPshotrs876658571
SNPdbers876658571
MSV3drs876658571
GWAS Ctlgrs876658571
Max Magnitude0
ClinVar
Risk rs876658571(T;T)
Alt rs876658571(T;T)
Reference rs876658571(C;C)
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.215657108G>A
CLNSRC
CLNACC RCV000219047.1,