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rs876659591

From SNPedia

Orientationminus
Geno Mag Summary
(TGAGGATTT;TGAGGATTT) 0 common in clinvar
Make rs876659591(CG;CG)
Make rs876659591(CG;TGAGGATTT)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093981
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659591
ebirs876659591
HLIrs876659591
Exacrs876659591
Varsomers876659591
Maprs876659591
PheGenIrs876659591
hapmaprs876659591
1000 genomesrs876659591
hgdprs876659591
ensemblrs876659591
gopubmedrs876659591
geneviewrs876659591
scholarrs876659591
googlers876659591
pharmgkbrs876659591
gwascentralrs876659591
openSNPrs876659591
23andMers876659591
23andMe allrs876659591
SNP Nexus

SNPshotrs876659591
SNPdbers876659591
MSV3drs876659591
GWAS Ctlgrs876659591
Max Magnitude0
ClinVar
Risk rs876659591(CG;CG)
Alt rs876659591(CG;CG)
Reference rs876659591(TGAGGATTT;TGAGGATTT)
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.41245998_41246006delAAATCCTCAinsCG
CLNSRC
CLNACC RCV000217286.1,