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rs876660043

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660043(-;-)
Make rs876660043(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32370426
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660043
dbSNP (old)rs876660043
ClinGenrs876660043
ebirs876660043
HLIrs876660043
Exacrs876660043
Gnomadrs876660043
Varsomers876660043
Maprs876660043
PheGenIrs876660043
Biobankrs876660043
1000 genomesrs876660043
hgdprs876660043
ensemblrs876660043
gopubmedrs876660043
geneviewrs876660043
scholarrs876660043
googlers876660043
pharmgkbrs876660043
gwascentralrs876660043
openSNPrs876660043
23andMers876660043
23andMe allrs876660043
SNP Nexus

SNPshotrs876660043
SNPdbers876660043
MSV3drs876660043
GWAS Ctlgrs876660043
Max Magnitude0
ClinVar
Risk rs876660043(-;-)
Alt rs876660043(-;-)
Reference Rs876660043(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32944563delG
CLNSRC
CLNACC RCV000216637.1,