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rs876660676

From SNPedia

Orientationplus
Geno Mag Summary
(AAAACGT;AAAACGT) 0 common in clinvar
Make rs876660676(-;-)
Make rs876660676(-;CGTAAAA)
Make rs876660676(CGTAAAA;CGTAAAA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340922
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660676
ebirs876660676
HLIrs876660676
Exacrs876660676
Varsomers876660676
Maprs876660676
PheGenIrs876660676
hapmaprs876660676
1000 genomesrs876660676
hgdprs876660676
ensemblrs876660676
gopubmedrs876660676
geneviewrs876660676
scholarrs876660676
googlers876660676
pharmgkbrs876660676
gwascentralrs876660676
openSNPrs876660676
23andMers876660676
23andMe allrs876660676
SNP Nexus

SNPshotrs876660676
SNPdbers876660676
MSV3drs876660676
GWAS Ctlgrs876660676
Max Magnitude0
ClinVar
Risk rs876660676(;)
Alt rs876660676(;)
Reference rs876660676(AAAACGT;AAAACGT)
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.32915059_32915065delCGTAAAA
CLNSRC
CLNACC RCV000219887.1,