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rs876661242

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661242(A;A)
Make rs876661242(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32394813
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876661242
ebirs876661242
HLIrs876661242
Exacrs876661242
Varsomers876661242
Maprs876661242
PheGenIrs876661242
hapmaprs876661242
1000 genomesrs876661242
hgdprs876661242
ensemblrs876661242
gopubmedrs876661242
geneviewrs876661242
scholarrs876661242
googlers876661242
pharmgkbrs876661242
gwascentralrs876661242
openSNPrs876661242
23andMers876661242
23andMe allrs876661242
SNP Nexus

SNPshotrs876661242
SNPdbers876661242
MSV3drs876661242
GWAS Ctlgrs876661242
Max Magnitude0
ClinVar
Risk rs876661242(A;A)
Alt rs876661242(A;A)
Reference rs876661242(G;G)
Significance Pathogenic
Disease not provided Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN not provided Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32968950G>A
CLNSRC
CLNACC RCV000219823.1, RCV000229281.1,