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rs80358092

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80358092(A;T)
Make rs80358092(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049088
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358092
ClinGenrs80358092
ebirs80358092
HLIrs80358092
Exacrs80358092
Varsomers80358092
Maprs80358092
PheGenIrs80358092
hapmaprs80358092
1000 genomesrs80358092
hgdprs80358092
ensemblrs80358092
gopubmedrs80358092
geneviewrs80358092
scholarrs80358092
googlers80358092
pharmgkbrs80358092
gwascentralrs80358092
openSNPrs80358092
23andMers80358092
23andMe allrs80358092
SNP Nexus

SNPshotrs80358092
SNPdbers80358092
MSV3drs80358092
GWAS Ctlgrs80358092
GMAF0.003214
Max Magnitude0
ClinVar
Risk rs80358092(T;T)
Alt rs80358092(T;T)
Reference Rs80358092(A;A)
Significance Non-pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41201105T>A
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048974.4, RCV000112635.4,