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rs876660911

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660911(-;-)
Make rs876660911(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214780604
GeneBARD1
is asnp
is mentioned by
dbSNPrs876660911
ebirs876660911
HLIrs876660911
Exacrs876660911
Varsomers876660911
Maprs876660911
PheGenIrs876660911
hapmaprs876660911
1000 genomesrs876660911
hgdprs876660911
ensemblrs876660911
gopubmedrs876660911
geneviewrs876660911
scholarrs876660911
googlers876660911
pharmgkbrs876660911
gwascentralrs876660911
openSNPrs876660911
23andMers876660911
23andMe allrs876660911
SNP Nexus

SNPshotrs876660911
SNPdbers876660911
MSV3drs876660911
GWAS Ctlgrs876660911
Max Magnitude0
ClinVar
Risk rs876660911(;)
Alt rs876660911(;)
Reference rs876660911(A;A)
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.215645328delT
CLNSRC
CLNACC RCV000218088.1,