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rs876659572

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659572(-;-)
Make rs876659572(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214745098
GeneBARD1
is asnp
is mentioned by
dbSNPrs876659572
ebirs876659572
HLIrs876659572
Exacrs876659572
Varsomers876659572
Maprs876659572
PheGenIrs876659572
hapmaprs876659572
1000 genomesrs876659572
hgdprs876659572
ensemblrs876659572
gopubmedrs876659572
geneviewrs876659572
scholarrs876659572
googlers876659572
pharmgkbrs876659572
gwascentralrs876659572
openSNPrs876659572
23andMers876659572
23andMe allrs876659572
SNP Nexus

SNPshotrs876659572
SNPdbers876659572
MSV3drs876659572
GWAS Ctlgrs876659572
Max Magnitude0
ClinVar
Risk rs876659572(;)
Alt rs876659572(;)
Reference rs876659572(T;T)
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.215609822delA
CLNSRC
CLNACC RCV000221033.1,