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rs876660390

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660390(-;-)
Make rs876660390(-;A)
Make rs876660390(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214769277
GeneBARD1
is asnp
is mentioned by
dbSNPrs876660390
ebirs876660390
HLIrs876660390
Exacrs876660390
Varsomers876660390
Maprs876660390
PheGenIrs876660390
hapmaprs876660390
1000 genomesrs876660390
hgdprs876660390
ensemblrs876660390
gopubmedrs876660390
geneviewrs876660390
scholarrs876660390
googlers876660390
pharmgkbrs876660390
gwascentralrs876660390
openSNPrs876660390
23andMers876660390
23andMe allrs876660390
SNP Nexus

SNPshotrs876660390
SNPdbers876660390
MSV3drs876660390
GWAS Ctlgrs876660390
Max Magnitude0
ClinVar
Risk rs876660390(A;A)
Alt rs876660390(A;A)
Reference rs876660390(;)
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.215634002dupT
CLNSRC
CLNACC RCV000213145.1,