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rs876661285

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661285(-;-)
Make rs876661285(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32396984
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876661285
ebirs876661285
HLIrs876661285
Exacrs876661285
Varsomers876661285
Maprs876661285
PheGenIrs876661285
hapmaprs876661285
1000 genomesrs876661285
hgdprs876661285
ensemblrs876661285
gopubmedrs876661285
geneviewrs876661285
scholarrs876661285
googlers876661285
pharmgkbrs876661285
gwascentralrs876661285
openSNPrs876661285
23andMers876661285
23andMe allrs876661285
SNP Nexus

SNPshotrs876661285
SNPdbers876661285
MSV3drs876661285
GWAS Ctlgrs876661285
Max Magnitude0
ClinVar
Risk rs876661285(;)
Alt rs876661285(;)
Reference rs876661285(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32971121delA
CLNSRC
CLNACC RCV000217863.1,