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rs876661236

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661236(-;-)
Make rs876661236(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340317
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876661236
ebirs876661236
HLIrs876661236
Exacrs876661236
Varsomers876661236
Maprs876661236
PheGenIrs876661236
hapmaprs876661236
1000 genomesrs876661236
hgdprs876661236
ensemblrs876661236
gopubmedrs876661236
geneviewrs876661236
scholarrs876661236
googlers876661236
pharmgkbrs876661236
gwascentralrs876661236
openSNPrs876661236
23andMers876661236
23andMe allrs876661236
SNP Nexus

SNPshotrs876661236
SNPdbers876661236
MSV3drs876661236
GWAS Ctlgrs876661236
Max Magnitude0
ClinVar
Risk rs876661236(;)
Alt rs876661236(;)
Reference rs876661236(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32914454delG
CLNSRC
CLNACC RCV000221517.1,