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rs876660305

From SNPedia

Orientationminus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs876660305(AC;T)
Make rs876660305(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093144
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876660305
ebirs876660305
HLIrs876660305
Exacrs876660305
Varsomers876660305
Maprs876660305
PheGenIrs876660305
hapmaprs876660305
1000 genomesrs876660305
hgdprs876660305
ensemblrs876660305
gopubmedrs876660305
geneviewrs876660305
scholarrs876660305
googlers876660305
pharmgkbrs876660305
gwascentralrs876660305
openSNPrs876660305
23andMers876660305
23andMe allrs876660305
SNP Nexus

SNPshotrs876660305
SNPdbers876660305
MSV3drs876660305
GWAS Ctlgrs876660305
Max Magnitude0
ClinVar
Risk rs876660305(T;T)
Alt rs876660305(T;T)
Reference rs876660305(AC;AC)
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.41245161_41245162delGTinsA
CLNSRC
CLNACC RCV000221355.1,