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rs80357227

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80357227(A;G)
Make rs80357227(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43057113
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357227
ebirs80357227
HLIrs80357227
Exacrs80357227
Varsomers80357227
Maprs80357227
PheGenIrs80357227
hapmaprs80357227
1000 genomesrs80357227
hgdprs80357227
ensemblrs80357227
gopubmedrs80357227
geneviewrs80357227
scholarrs80357227
googlers80357227
pharmgkbrs80357227
gwascentralrs80357227
openSNPrs80357227
23andMers80357227
23andMe allrs80357227
SNP Nexus

SNPshotrs80357227
SNPdbers80357227
MSV3drs80357227
GWAS Ctlgrs80357227
Max Magnitude0
ClinVar
Risk rs80357227(G,T;G,T)
Alt rs80357227(G,T;G,T)
Reference rs80357227(A;A)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41209130T>A; NC_000017.10:g.41209130T>C
CLNSRC ClinVar
CLNACC RCV000048868.2, RCV000048867.2, RCV000112569.1,