Have questions? Visit https://www.reddit.com/r/SNPedia

rs876659878

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659878(G;T)
Make rs876659878(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43076540
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659878
ebirs876659878
HLIrs876659878
Exacrs876659878
Varsomers876659878
Maprs876659878
PheGenIrs876659878
hapmaprs876659878
1000 genomesrs876659878
hgdprs876659878
ensemblrs876659878
gopubmedrs876659878
geneviewrs876659878
scholarrs876659878
googlers876659878
pharmgkbrs876659878
gwascentralrs876659878
openSNPrs876659878
23andMers876659878
23andMe allrs876659878
SNP Nexus

SNPshotrs876659878
SNPdbers876659878
MSV3drs876659878
GWAS Ctlgrs876659878
Max Magnitude0
ClinVar
Risk rs876659878(T;T)
Alt rs876659878(T;T)
Reference rs876659878(G;G)
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.41228557C>A
CLNSRC
CLNACC RCV000216843.1,