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rs876658618

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs876658618(-;-)
Make rs876658618(-;TA)
Make rs876658618(TA;TA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32337612
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658618
ebirs876658618
HLIrs876658618
Exacrs876658618
Varsomers876658618
Maprs876658618
PheGenIrs876658618
hapmaprs876658618
1000 genomesrs876658618
hgdprs876658618
ensemblrs876658618
gopubmedrs876658618
geneviewrs876658618
scholarrs876658618
googlers876658618
pharmgkbrs876658618
gwascentralrs876658618
openSNPrs876658618
23andMers876658618
23andMe allrs876658618
SNP Nexus

SNPshotrs876658618
SNPdbers876658618
MSV3drs876658618
GWAS Ctlgrs876658618
Max Magnitude0
ClinVar
Risk rs876658618(;)
Alt rs876658618(;)
Reference rs876658618(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.32911749_32911750delTA
CLNSRC
CLNACC RCV000218983.1,