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rs876659229

From SNPedia

Orientationplus
Geno Mag Summary
(GATA;GATA) 0 common in clinvar
Make rs876659229(-;-)
Make rs876659229(-;AGAT)
Make rs876659229(AGAT;AGAT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32356426
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659229
ebirs876659229
HLIrs876659229
Exacrs876659229
Varsomers876659229
Maprs876659229
PheGenIrs876659229
hapmaprs876659229
1000 genomesrs876659229
hgdprs876659229
ensemblrs876659229
gopubmedrs876659229
geneviewrs876659229
scholarrs876659229
googlers876659229
pharmgkbrs876659229
gwascentralrs876659229
openSNPrs876659229
23andMers876659229
23andMe allrs876659229
SNP Nexus

SNPshotrs876659229
SNPdbers876659229
MSV3drs876659229
GWAS Ctlgrs876659229
Max Magnitude0
ClinVar
Risk rs876659229(;)
Alt rs876659229(;)
Reference rs876659229(GATA;GATA)
Significance Probable-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.32930563_32930566delAGAT
CLNSRC
CLNACC RCV000215010.1,