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rs876658905

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658905(A;A)
Make rs876658905(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214792446
GeneBARD1
is asnp
is mentioned by
dbSNPrs876658905
ebirs876658905
HLIrs876658905
Exacrs876658905
Varsomers876658905
Maprs876658905
PheGenIrs876658905
hapmaprs876658905
1000 genomesrs876658905
hgdprs876658905
ensemblrs876658905
gopubmedrs876658905
geneviewrs876658905
scholarrs876658905
googlers876658905
pharmgkbrs876658905
gwascentralrs876658905
openSNPrs876658905
23andMers876658905
23andMe allrs876658905
SNP Nexus

SNPshotrs876658905
SNPdbers876658905
MSV3drs876658905
GWAS Ctlgrs876658905
Max Magnitude0
ClinVar
Risk rs876658905(A;A)
Alt rs876658905(A;A)
Reference rs876658905(G;G)
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.215657170C>T
CLNSRC
CLNACC RCV000217544.1,