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rs77202719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs77202719(-;-)
Make rs77202719(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340299
GeneBRCA2
is asnp
is mentioned by
dbSNPrs77202719
ebirs77202719
HLIrs77202719
Exacrs77202719
Varsomers77202719
Maprs77202719
PheGenIrs77202719
hapmaprs77202719
1000 genomesrs77202719
hgdprs77202719
ensemblrs77202719
gopubmedrs77202719
geneviewrs77202719
scholarrs77202719
googlers77202719
pharmgkbrs77202719
gwascentralrs77202719
openSNPrs77202719
23andMers77202719
23andMe allrs77202719
SNP Nexus

SNPshotrs77202719
SNPdbers77202719
MSV3drs77202719
GWAS Ctlgrs77202719
Max Magnitude0
ClinVar
Risk rs77202719(;)
Alt rs77202719(;)
Reference rs77202719(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000013.11:g.32340299delA
CLNSRC ClinVar
CLNACC RCV000044795.2,