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rs876659047

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs876659047(AT;AT)
Make rs876659047(AT;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32380084
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659047
ebirs876659047
HLIrs876659047
Exacrs876659047
Varsomers876659047
Maprs876659047
PheGenIrs876659047
hapmaprs876659047
1000 genomesrs876659047
hgdprs876659047
ensemblrs876659047
gopubmedrs876659047
geneviewrs876659047
scholarrs876659047
googlers876659047
pharmgkbrs876659047
gwascentralrs876659047
openSNPrs876659047
23andMers876659047
23andMe allrs876659047
SNP Nexus

SNPshotrs876659047
SNPdbers876659047
MSV3drs876659047
GWAS Ctlgrs876659047
Max Magnitude0
ClinVar
Risk rs876659047(AT;AT)
Alt rs876659047(AT;AT)
Reference rs876659047(TC;TC)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32954221_32954222delTCinsAT
CLNSRC
CLNACC RCV000215926.1, RCV000229620.1,