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rs876659865

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659865(-;-)
Make rs876659865(-;AACA)
Make rs876659865(AACA;AACA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43091596
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659865
ebirs876659865
HLIrs876659865
Exacrs876659865
Varsomers876659865
Maprs876659865
PheGenIrs876659865
hapmaprs876659865
1000 genomesrs876659865
hgdprs876659865
ensemblrs876659865
gopubmedrs876659865
geneviewrs876659865
scholarrs876659865
googlers876659865
pharmgkbrs876659865
gwascentralrs876659865
openSNPrs876659865
23andMers876659865
23andMe allrs876659865
SNP Nexus

SNPshotrs876659865
SNPdbers876659865
MSV3drs876659865
GWAS Ctlgrs876659865
Max Magnitude0
ClinVar
Risk rs876659865(AACA;AACA)
Alt rs876659865(AACA;AACA)
Reference rs876659865(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.41243614_41243617dupTGTT
CLNSRC
CLNACC RCV000219345.1,