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rs876658672

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;G) 6 BRCA1 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs876658672(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43063891
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876658672
dbSNP (old)rs876658672
ClinGenrs876658672
ebirs876658672
HLIrs876658672
Exacrs876658672
Gnomadrs876658672
Varsomers876658672
Maprs876658672
PheGenIrs876658672
Biobankrs876658672
1000 genomesrs876658672
hgdprs876658672
ensemblrs876658672
gopubmedrs876658672
geneviewrs876658672
scholarrs876658672
googlers876658672
pharmgkbrs876658672
gwascentralrs876658672
openSNPrs876658672
23andMers876658672
23andMe allrs876658672
SNP Nexus

SNPshotrs876658672
SNPdbers876658672
MSV3drs876658672
GWAS Ctlgrs876658672
Max Magnitude6
ClinVar
Risk rs876658672(A;A)
Alt rs876658672(A;A)
Reference Rs876658672(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41215908C>T
CLNSRC
CLNACC RCV000223034.1, RCV000257427.2,