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rs876659752

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs876659752(-;-)
Make rs876659752(-;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214781035
GeneBARD1
is asnp
is mentioned by
dbSNPrs876659752
ebirs876659752
HLIrs876659752
Exacrs876659752
Varsomers876659752
Maprs876659752
PheGenIrs876659752
hapmaprs876659752
1000 genomesrs876659752
hgdprs876659752
ensemblrs876659752
gopubmedrs876659752
geneviewrs876659752
scholarrs876659752
googlers876659752
pharmgkbrs876659752
gwascentralrs876659752
openSNPrs876659752
23andMers876659752
23andMe allrs876659752
SNP Nexus

SNPshotrs876659752
SNPdbers876659752
MSV3drs876659752
GWAS Ctlgrs876659752
Max Magnitude0
ClinVar
Risk rs876659752(;)
Alt rs876659752(;)
Reference rs876659752(TT;TT)
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.215645759_215645760delAA
CLNSRC
CLNACC RCV000219768.1,