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rs876659867

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659867(-;-)
Make rs876659867(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43057127
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659867
ebirs876659867
HLIrs876659867
Exacrs876659867
Varsomers876659867
Maprs876659867
PheGenIrs876659867
hapmaprs876659867
1000 genomesrs876659867
hgdprs876659867
ensemblrs876659867
gopubmedrs876659867
geneviewrs876659867
scholarrs876659867
googlers876659867
pharmgkbrs876659867
gwascentralrs876659867
openSNPrs876659867
23andMers876659867
23andMe allrs876659867
SNP Nexus

SNPshotrs876659867
SNPdbers876659867
MSV3drs876659867
GWAS Ctlgrs876659867
Max Magnitude0
ClinVar
Risk rs876659867(;)
Alt rs876659867(;)
Reference rs876659867(T;T)
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.41209144delA
CLNSRC
CLNACC RCV000219797.1,