Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853568

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs878853568(-;-)
Make rs878853568(-;TA)
Make rs878853568(TA;TA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32325101
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853568
ebirs878853568
HLIrs878853568
Exacrs878853568
Varsomers878853568
Maprs878853568
PheGenIrs878853568
hapmaprs878853568
1000 genomesrs878853568
hgdprs878853568
ensemblrs878853568
gopubmedrs878853568
geneviewrs878853568
scholarrs878853568
googlers878853568
pharmgkbrs878853568
gwascentralrs878853568
openSNPrs878853568
23andMers878853568
23andMe allrs878853568
SNP Nexus

SNPshotrs878853568
SNPdbers878853568
MSV3drs878853568
GWAS Ctlgrs878853568
Max Magnitude0
ClinVar
Risk rs878853568(;)
Alt rs878853568(;)
Reference rs878853568(AT;AT)
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.32899238_32899239delTA
CLNSRC
CLNACC RCV000233383.1,