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rs876659100

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659100(A;T)
Make rs876659100(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32330958
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659100
ebirs876659100
HLIrs876659100
Exacrs876659100
Varsomers876659100
Maprs876659100
PheGenIrs876659100
hapmaprs876659100
1000 genomesrs876659100
hgdprs876659100
ensemblrs876659100
gopubmedrs876659100
geneviewrs876659100
scholarrs876659100
googlers876659100
pharmgkbrs876659100
gwascentralrs876659100
openSNPrs876659100
23andMers876659100
23andMe allrs876659100
SNP Nexus

SNPshotrs876659100
SNPdbers876659100
MSV3drs876659100
GWAS Ctlgrs876659100
Max Magnitude0
ClinVar
Risk rs876659100(T;T)
Alt rs876659100(T;T)
Reference rs876659100(A;A)
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.32905095A>T
CLNSRC
CLNACC RCV000219810.1,