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

rs876660425

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660425(-;-)
Make rs876660425(-;C)
Make rs876660425(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43092864
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876660425
ebirs876660425
HLIrs876660425
Exacrs876660425
Varsomers876660425
Maprs876660425
PheGenIrs876660425
hapmaprs876660425
1000 genomesrs876660425
hgdprs876660425
ensemblrs876660425
gopubmedrs876660425
geneviewrs876660425
scholarrs876660425
googlers876660425
pharmgkbrs876660425
gwascentralrs876660425
openSNPrs876660425
23andMers876660425
23andMe allrs876660425
SNP Nexus

SNPshotrs876660425
SNPdbers876660425
MSV3drs876660425
GWAS Ctlgrs876660425
Max Magnitude0
ClinVar
Risk rs876660425(C;C)
Alt rs876660425(C;C)
Reference rs876660425(;)
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.41244882dupG
CLNSRC
CLNACC RCV000218586.1,