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rs80357112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80357112(A;A)
Make rs80357112(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051063
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357112
ebirs80357112
HLIrs80357112
Exacrs80357112
Varsomers80357112
Maprs80357112
PheGenIrs80357112
hapmaprs80357112
1000 genomesrs80357112
hgdprs80357112
ensemblrs80357112
gopubmedrs80357112
geneviewrs80357112
scholarrs80357112
googlers80357112
pharmgkbrs80357112
gwascentralrs80357112
openSNPrs80357112
23andMers80357112
23andMe allrs80357112
SNP Nexus

SNPshotrs80357112
SNPdbers80357112
MSV3drs80357112
GWAS Ctlgrs80357112
Max Magnitude0
ClinVar
Risk rs80357112(A,C,T;A,C,T)
Alt rs80357112(A,C,T;A,C,T)
Reference rs80357112(G;G)
Significance Untested
Disease Familial cancer of breast Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000017.10:g.41203080C>A; NC_000017.10:g.41203080C>G; NC_000017.10:g.41203080C>T
CLNSRC ClinVar Ambry Genetics
CLNACC RCV000048938.2, RCV000048937.2, RCV000048936.3, RCV000077615.3, RCV000131398.2, RCV000235603.1,