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rs80357243

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80357243(G;G)
Make rs80357243(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063885
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357243
ebirs80357243
HLIrs80357243
Exacrs80357243
Varsomers80357243
Maprs80357243
PheGenIrs80357243
hapmaprs80357243
1000 genomesrs80357243
hgdprs80357243
ensemblrs80357243
gopubmedrs80357243
geneviewrs80357243
scholarrs80357243
googlers80357243
pharmgkbrs80357243
gwascentralrs80357243
openSNPrs80357243
23andMers80357243
23andMe allrs80357243
SNP Nexus

SNPshotrs80357243
SNPdbers80357243
MSV3drs80357243
GWAS Ctlgrs80357243
Max Magnitude0
ClinVar
Risk rs80357243(G;G)
Alt rs80357243(G;G)
Reference rs80357243(T;T)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41215902A>C
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000048809.2, RCV000112504.1, RCV000129696.2,