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rs876658790

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658790(A;A)
Make rs876658790(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43076615
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876658790
ebirs876658790
HLIrs876658790
Exacrs876658790
Varsomers876658790
Maprs876658790
PheGenIrs876658790
hapmaprs876658790
1000 genomesrs876658790
hgdprs876658790
ensemblrs876658790
gopubmedrs876658790
geneviewrs876658790
scholarrs876658790
googlers876658790
pharmgkbrs876658790
gwascentralrs876658790
openSNPrs876658790
23andMers876658790
23andMe allrs876658790
SNP Nexus

SNPshotrs876658790
SNPdbers876658790
MSV3drs876658790
GWAS Ctlgrs876658790
Max Magnitude0
ClinVar
Risk rs876658790(A;A)
Alt rs876658790(A;A)
Reference rs876658790(G;G)
Significance Probable-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.41228632C>T
CLNSRC
CLNACC RCV000216055.1,