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rs876658260

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658260(A;T)
Make rs876658260(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214729010
GeneBARD1
is asnp
is mentioned by
dbSNPrs876658260
ebirs876658260
HLIrs876658260
Exacrs876658260
Varsomers876658260
Maprs876658260
PheGenIrs876658260
hapmaprs876658260
1000 genomesrs876658260
hgdprs876658260
ensemblrs876658260
gopubmedrs876658260
geneviewrs876658260
scholarrs876658260
googlers876658260
pharmgkbrs876658260
gwascentralrs876658260
openSNPrs876658260
23andMers876658260
23andMe allrs876658260
SNP Nexus

SNPshotrs876658260
SNPdbers876658260
MSV3drs876658260
GWAS Ctlgrs876658260
Max Magnitude0
ClinVar
Risk rs876658260(T;T)
Alt rs876658260(T;T)
Reference rs876658260(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.215593734T>A
CLNSRC
CLNACC RCV000217545.1,