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

rs876659396

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659396(-;-)
Make rs876659396(-;TC)
Make rs876659396(TC;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43094425
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659396
ebirs876659396
HLIrs876659396
Exacrs876659396
Varsomers876659396
Maprs876659396
PheGenIrs876659396
hapmaprs876659396
1000 genomesrs876659396
hgdprs876659396
ensemblrs876659396
gopubmedrs876659396
geneviewrs876659396
scholarrs876659396
googlers876659396
pharmgkbrs876659396
gwascentralrs876659396
openSNPrs876659396
23andMers876659396
23andMe allrs876659396
SNP Nexus

SNPshotrs876659396
SNPdbers876659396
MSV3drs876659396
GWAS Ctlgrs876659396
Max Magnitude0
ClinVar
Risk rs876659396(TC;TC)
Alt rs876659396(TC;TC)
Reference rs876659396(;)
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.41246442_41246443insGA
CLNSRC
CLNACC RCV000223080.1,