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rs876658672

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658672(A;A)
Make rs876658672(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43063891
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876658672
ebirs876658672
HLIrs876658672
Exacrs876658672
Varsomers876658672
Maprs876658672
PheGenIrs876658672
hapmaprs876658672
1000 genomesrs876658672
hgdprs876658672
ensemblrs876658672
gopubmedrs876658672
geneviewrs876658672
scholarrs876658672
googlers876658672
pharmgkbrs876658672
gwascentralrs876658672
openSNPrs876658672
23andMers876658672
23andMe allrs876658672
SNP Nexus

SNPshotrs876658672
SNPdbers876658672
MSV3drs876658672
GWAS Ctlgrs876658672
Max Magnitude0
ClinVar
Risk rs876658672(A;A)
Alt rs876658672(A;A)
Reference rs876658672(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.41215908C>T
CLNSRC
CLNACC RCV000223034.1,