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

rs876658478

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658478(-;-)
Make rs876658478(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43063350
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876658478
ebirs876658478
HLIrs876658478
Exacrs876658478
Varsomers876658478
Maprs876658478
PheGenIrs876658478
hapmaprs876658478
1000 genomesrs876658478
hgdprs876658478
ensemblrs876658478
gopubmedrs876658478
geneviewrs876658478
scholarrs876658478
googlers876658478
pharmgkbrs876658478
gwascentralrs876658478
openSNPrs876658478
23andMers876658478
23andMe allrs876658478
SNP Nexus

SNPshotrs876658478
SNPdbers876658478
MSV3drs876658478
GWAS Ctlgrs876658478
Max Magnitude0
ClinVar
Risk rs876658478(;)
Alt rs876658478(;)
Reference rs876658478(A;A)
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.41215367delT
CLNSRC
CLNACC RCV000216416.1,