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rs876659894

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659894(A;A)
Make rs876659894(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214745721
GeneBARD1
is asnp
is mentioned by
dbSNPrs876659894
ebirs876659894
HLIrs876659894
Exacrs876659894
Varsomers876659894
Maprs876659894
PheGenIrs876659894
hapmaprs876659894
1000 genomesrs876659894
hgdprs876659894
ensemblrs876659894
gopubmedrs876659894
geneviewrs876659894
scholarrs876659894
googlers876659894
pharmgkbrs876659894
gwascentralrs876659894
openSNPrs876659894
23andMers876659894
23andMe allrs876659894
SNP Nexus

SNPshotrs876659894
SNPdbers876659894
MSV3drs876659894
GWAS Ctlgrs876659894
Max Magnitude0
ClinVar
Risk rs876659894(A;A)
Alt rs876659894(A;A)
Reference rs876659894(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.215610445C>T
CLNSRC
CLNACC RCV000215189.1,