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rs876660761

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660761(-;-)
Make rs876660761(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214781282
GeneBARD1
is asnp
is mentioned by
dbSNPrs876660761
ebirs876660761
HLIrs876660761
Exacrs876660761
Varsomers876660761
Maprs876660761
PheGenIrs876660761
hapmaprs876660761
1000 genomesrs876660761
hgdprs876660761
ensemblrs876660761
gopubmedrs876660761
geneviewrs876660761
scholarrs876660761
googlers876660761
pharmgkbrs876660761
gwascentralrs876660761
openSNPrs876660761
23andMers876660761
23andMe allrs876660761
SNP Nexus

SNPshotrs876660761
SNPdbers876660761
MSV3drs876660761
GWAS Ctlgrs876660761
Max Magnitude0
ClinVar
Risk rs876660761(;)
Alt rs876660761(;)
Reference rs876660761(G;G)
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.215646006delC
CLNSRC
CLNACC RCV000219761.1,