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rs377698594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377698594(C;T)
Make rs377698594(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341155
GeneBRCA2
is asnp
is mentioned by
dbSNPrs377698594
ebirs377698594
HLIrs377698594
Exacrs377698594
Varsomers377698594
Maprs377698594
PheGenIrs377698594
hapmaprs377698594
1000 genomesrs377698594
hgdprs377698594
ensemblrs377698594
gopubmedrs377698594
geneviewrs377698594
scholarrs377698594
googlers377698594
pharmgkbrs377698594
gwascentralrs377698594
openSNPrs377698594
23andMers377698594
23andMe allrs377698594
SNP Nexus

SNPshotrs377698594
SNPdbers377698594
MSV3drs377698594
GWAS Ctlgrs377698594
Max Magnitude0
ClinVar
Risk rs377698594(A,T;A,T)
Alt rs377698594(A,T;A,T)
Reference rs377698594(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32915292C>A
CLNSRC ClinVar
CLNACC RCV000045054.2,