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rs876659100

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs876659100(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32330958
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659100
dbSNP (old)rs876659100
ClinGenrs876659100
ebirs876659100
HLIrs876659100
Exacrs876659100
Gnomadrs876659100
Varsomers876659100
Maprs876659100
PheGenIrs876659100
Biobankrs876659100
1000 genomesrs876659100
hgdprs876659100
ensemblrs876659100
gopubmedrs876659100
geneviewrs876659100
scholarrs876659100
googlers876659100
pharmgkbrs876659100
gwascentralrs876659100
openSNPrs876659100
23andMers876659100
23andMe allrs876659100
SNP Nexus

SNPshotrs876659100
SNPdbers876659100
MSV3drs876659100
GWAS Ctlgrs876659100
Max Magnitude6
ClinVar
Risk rs876659100(T;T)
Alt rs876659100(T;T)
Reference Rs876659100(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32905095A>T
CLNSRC
CLNACC RCV000219810.1, RCV000240982.1,