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rs876659483

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659483(-;-)
Make rs876659483(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43057093
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659483
ebirs876659483
HLIrs876659483
Exacrs876659483
Varsomers876659483
Maprs876659483
PheGenIrs876659483
hapmaprs876659483
1000 genomesrs876659483
hgdprs876659483
ensemblrs876659483
gopubmedrs876659483
geneviewrs876659483
scholarrs876659483
googlers876659483
pharmgkbrs876659483
gwascentralrs876659483
openSNPrs876659483
23andMers876659483
23andMe allrs876659483
SNP Nexus

SNPshotrs876659483
SNPdbers876659483
MSV3drs876659483
GWAS Ctlgrs876659483
Max Magnitude0
ClinVar
Risk rs876659483(;)
Alt rs876659483(;)
Reference rs876659483(C;C)
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.41209110delG
CLNSRC
CLNACC RCV000217835.1,