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rs878853579

From SNPedia

Orientationplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs878853579(-;-)
Make rs878853579(-;GG)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338525
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853579
ebirs878853579
HLIrs878853579
Exacrs878853579
Varsomers878853579
Maprs878853579
PheGenIrs878853579
hapmaprs878853579
1000 genomesrs878853579
hgdprs878853579
ensemblrs878853579
gopubmedrs878853579
geneviewrs878853579
scholarrs878853579
googlers878853579
pharmgkbrs878853579
gwascentralrs878853579
openSNPrs878853579
23andMers878853579
23andMe allrs878853579
SNP Nexus

SNPshotrs878853579
SNPdbers878853579
MSV3drs878853579
GWAS Ctlgrs878853579
Max Magnitude0
ClinVar
Risk rs878853579(;)
Alt rs878853579(;)
Reference rs878853579(GG;GG)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32912662_32912663delGG
CLNSRC
CLNACC RCV000227031.1,