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rs876660563

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs876660563(-;-)
Make rs876660563(-;TA)
Make rs876660563(TA;TA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32355194
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660563
ebirs876660563
HLIrs876660563
Exacrs876660563
Varsomers876660563
Maprs876660563
PheGenIrs876660563
hapmaprs876660563
1000 genomesrs876660563
hgdprs876660563
ensemblrs876660563
gopubmedrs876660563
geneviewrs876660563
scholarrs876660563
googlers876660563
pharmgkbrs876660563
gwascentralrs876660563
openSNPrs876660563
23andMers876660563
23andMe allrs876660563
SNP Nexus

SNPshotrs876660563
SNPdbers876660563
MSV3drs876660563
GWAS Ctlgrs876660563
Max Magnitude0
ClinVar
Risk rs876660563(;)
Alt rs876660563(;)
Reference rs876660563(AT;AT)
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.32929331_32929332delTA
CLNSRC
CLNACC RCV000213613.1,