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rs876660282

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660282(A;T)
Make rs876660282(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093430
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876660282
ebirs876660282
HLIrs876660282
Exacrs876660282
Varsomers876660282
Maprs876660282
PheGenIrs876660282
hapmaprs876660282
1000 genomesrs876660282
hgdprs876660282
ensemblrs876660282
gopubmedrs876660282
geneviewrs876660282
scholarrs876660282
googlers876660282
pharmgkbrs876660282
gwascentralrs876660282
openSNPrs876660282
23andMers876660282
23andMe allrs876660282
SNP Nexus

SNPshotrs876660282
SNPdbers876660282
MSV3drs876660282
GWAS Ctlgrs876660282
Max Magnitude0
ClinVar
Risk rs876660282(T;T)
Alt rs876660282(T;T)
Reference rs876660282(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.41245447T>A
CLNSRC
CLNACC RCV000218292.1,