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rs80357214

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80357214(G;G)
Make rs80357214(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094739
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357214
ebirs80357214
HLIrs80357214
Exacrs80357214
Varsomers80357214
Maprs80357214
PheGenIrs80357214
hapmaprs80357214
1000 genomesrs80357214
hgdprs80357214
ensemblrs80357214
gopubmedrs80357214
geneviewrs80357214
scholarrs80357214
googlers80357214
pharmgkbrs80357214
gwascentralrs80357214
openSNPrs80357214
23andMers80357214
23andMe allrs80357214
SNP Nexus

SNPshotrs80357214
SNPdbers80357214
MSV3drs80357214
GWAS Ctlgrs80357214
Max Magnitude0
ClinVar
Risk rs80357214(G;G)
Alt rs80357214(G;G)
Reference rs80357214(T;T)
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.41246756A>C
CLNSRC ClinVar
CLNACC RCV000049138.2, RCV000112787.1,