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

rs876659211

From SNPedia

Orientationplus
Geno Mag Summary
(CTTA;CTTA) 0 common in clinvar
Make rs876659211(-;-)
Make rs876659211(-;ACTT)
Make rs876659211(ACTT;ACTT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32394841
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659211
ebirs876659211
HLIrs876659211
Exacrs876659211
Varsomers876659211
Maprs876659211
PheGenIrs876659211
hapmaprs876659211
1000 genomesrs876659211
hgdprs876659211
ensemblrs876659211
gopubmedrs876659211
geneviewrs876659211
scholarrs876659211
googlers876659211
pharmgkbrs876659211
gwascentralrs876659211
openSNPrs876659211
23andMers876659211
23andMe allrs876659211
SNP Nexus

SNPshotrs876659211
SNPdbers876659211
MSV3drs876659211
GWAS Ctlgrs876659211
Max Magnitude0
ClinVar
Risk rs876659211(;)
Alt rs876659211(;)
Reference rs876659211(CTTA;CTTA)
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.32968978_32968981delACTT
CLNSRC
CLNACC RCV000219908.1, RCV000233261.1,