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rs876659867

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659867(-;-)
Make rs876659867(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43057127
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659867
dbSNP (classic)rs876659867
ClinGenrs876659867
ebirs876659867
HLIrs876659867
Exacrs876659867
Gnomadrs876659867
Varsomers876659867
LitVarrs876659867
Maprs876659867
PheGenIrs876659867
Biobankrs876659867
1000 genomesrs876659867
hgdprs876659867
ensemblrs876659867
geneviewrs876659867
scholarrs876659867
googlers876659867
pharmgkbrs876659867
gwascentralrs876659867
openSNPrs876659867
23andMers876659867
SNPshotrs876659867
SNPdbers876659867
MSV3drs876659867
GWAS Ctlgrs876659867
Max Magnitude0
ClinVar
Risk rs876659867(-;-)
Alt rs876659867(-;-)
Reference Rs876659867(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41209144delA
CLNSRC
CLNACC RCV000219797.1,