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rs876658850

From SNPedia

Orientationplus
Geno Mag Summary
(TCTTG;TCTTG) 0 common in clinvar
Make rs876658850(-;-)
Make rs876658850(-;GTCTT)
Make rs876658850(GTCTT;GTCTT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32325172
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658850
ebirs876658850
HLIrs876658850
Exacrs876658850
Varsomers876658850
Maprs876658850
PheGenIrs876658850
hapmaprs876658850
1000 genomesrs876658850
hgdprs876658850
ensemblrs876658850
gopubmedrs876658850
geneviewrs876658850
scholarrs876658850
googlers876658850
pharmgkbrs876658850
gwascentralrs876658850
openSNPrs876658850
23andMers876658850
23andMe allrs876658850
SNP Nexus

SNPshotrs876658850
SNPdbers876658850
MSV3drs876658850
GWAS Ctlgrs876658850
Max Magnitude0
ClinVar
Risk rs876658850(;)
Alt rs876658850(;)
Reference rs876658850(TCTTG;TCTTG)
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.32899309_32899313delGTCTT
CLNSRC
CLNACC RCV000219602.1,