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rs876660385

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660385(-;-)
Make rs876660385(-;CAAT)
Make rs876660385(CAAT;CAAT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32332338
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660385
ebirs876660385
HLIrs876660385
Exacrs876660385
Varsomers876660385
Maprs876660385
PheGenIrs876660385
hapmaprs876660385
1000 genomesrs876660385
hgdprs876660385
ensemblrs876660385
gopubmedrs876660385
geneviewrs876660385
scholarrs876660385
googlers876660385
pharmgkbrs876660385
gwascentralrs876660385
openSNPrs876660385
23andMers876660385
23andMe allrs876660385
SNP Nexus

SNPshotrs876660385
SNPdbers876660385
MSV3drs876660385
GWAS Ctlgrs876660385
Max Magnitude0
ClinVar
Risk rs876660385(TCAA;TCAA)
Alt rs876660385(TCAA;TCAA)
Reference rs876660385(;)
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.32906472_32906475dupCAAT
CLNSRC
CLNACC RCV000216716.1,