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rs876660287

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660287(-;-)
Make rs876660287(-;AT)
Make rs876660287(AT;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32398230
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660287
ebirs876660287
HLIrs876660287
Exacrs876660287
Varsomers876660287
Maprs876660287
PheGenIrs876660287
hapmaprs876660287
1000 genomesrs876660287
hgdprs876660287
ensemblrs876660287
gopubmedrs876660287
geneviewrs876660287
scholarrs876660287
googlers876660287
pharmgkbrs876660287
gwascentralrs876660287
openSNPrs876660287
23andMers876660287
23andMe allrs876660287
SNP Nexus

SNPshotrs876660287
SNPdbers876660287
MSV3drs876660287
GWAS Ctlgrs876660287
Max Magnitude0
ClinVar
Risk rs876660287(TA;TA)
Alt rs876660287(TA;TA)
Reference rs876660287(;)
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.32972367_32972368insAT
CLNSRC
CLNACC RCV000218421.1,