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rs876659656

From SNPedia

Orientationplus
Geno Mag Summary
(AATG;AATG) 0 common in clinvar
Make rs876659656(-;-)
Make rs876659656(-;TGAA)
Make rs876659656(TGAA;TGAA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32337991
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659656
ebirs876659656
HLIrs876659656
Exacrs876659656
Varsomers876659656
Maprs876659656
PheGenIrs876659656
hapmaprs876659656
1000 genomesrs876659656
hgdprs876659656
ensemblrs876659656
gopubmedrs876659656
geneviewrs876659656
scholarrs876659656
googlers876659656
pharmgkbrs876659656
gwascentralrs876659656
openSNPrs876659656
23andMers876659656
23andMe allrs876659656
SNP Nexus

SNPshotrs876659656
SNPdbers876659656
MSV3drs876659656
GWAS Ctlgrs876659656
Max Magnitude0
ClinVar
Risk rs876659656(;)
Alt rs876659656(;)
Reference rs876659656(AATG;AATG)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32912128_32912131delTGAA
CLNSRC
CLNACC RCV000217645.1,