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rs876661270

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs876661270(-;-)
Make rs876661270(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32337414
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876661270
ebirs876661270
HLIrs876661270
Exacrs876661270
Varsomers876661270
Maprs876661270
PheGenIrs876661270
hapmaprs876661270
1000 genomesrs876661270
hgdprs876661270
ensemblrs876661270
gopubmedrs876661270
geneviewrs876661270
scholarrs876661270
googlers876661270
pharmgkbrs876661270
gwascentralrs876661270
openSNPrs876661270
23andMers876661270
23andMe allrs876661270
SNP Nexus

SNPshotrs876661270
SNPdbers876661270
MSV3drs876661270
GWAS Ctlgrs876661270
Max Magnitude0
ClinVar
Risk rs876661270(;)
Alt rs876661270(;)
Reference rs876661270(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32911551_32911552delCT
CLNSRC
CLNACC RCV000217537.1,