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rs876661023

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs876661023(-;-)
Make rs876661023(-;GA)
Make rs876661023(GA;GA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32379810
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876661023
ebirs876661023
HLIrs876661023
Exacrs876661023
Varsomers876661023
Maprs876661023
PheGenIrs876661023
hapmaprs876661023
1000 genomesrs876661023
hgdprs876661023
ensemblrs876661023
gopubmedrs876661023
geneviewrs876661023
scholarrs876661023
googlers876661023
pharmgkbrs876661023
gwascentralrs876661023
openSNPrs876661023
23andMers876661023
23andMe allrs876661023
SNP Nexus

SNPshotrs876661023
SNPdbers876661023
MSV3drs876661023
GWAS Ctlgrs876661023
Max Magnitude0
ClinVar
Risk rs876661023(;)
Alt rs876661023(;)
Reference rs876661023(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32953947_32953948delGA
CLNSRC
CLNACC RCV000215223.1,