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rs876659447

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659447(-;-)
Make rs876659447(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093129
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659447
ebirs876659447
HLIrs876659447
Exacrs876659447
Varsomers876659447
Maprs876659447
PheGenIrs876659447
hapmaprs876659447
1000 genomesrs876659447
hgdprs876659447
ensemblrs876659447
gopubmedrs876659447
geneviewrs876659447
scholarrs876659447
googlers876659447
pharmgkbrs876659447
gwascentralrs876659447
openSNPrs876659447
23andMers876659447
23andMe allrs876659447
SNP Nexus

SNPshotrs876659447
SNPdbers876659447
MSV3drs876659447
GWAS Ctlgrs876659447
Max Magnitude0
ClinVar
Risk rs876659447(;)
Alt rs876659447(;)
Reference rs876659447(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.41245146delC
CLNSRC
CLNACC RCV000213419.1,