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rs80357368

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80357368(A;A)
Make rs80357368(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045748
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357368
dbSNP (classic)rs80357368
ClinGenrs80357368
ebirs80357368
HLIrs80357368
Exacrs80357368
Gnomadrs80357368
Varsomers80357368
LitVarrs80357368
Maprs80357368
PheGenIrs80357368
Biobankrs80357368
1000 genomesrs80357368
hgdprs80357368
ensemblrs80357368
geneviewrs80357368
scholarrs80357368
googlers80357368
pharmgkbrs80357368
gwascentralrs80357368
openSNPrs80357368
23andMers80357368
SNPshotrs80357368
SNPdbers80357368
MSV3drs80357368
GWAS Ctlgrs80357368
Max Magnitude0
ClinVar
Risk rs80357368(A;A) rs80357368(C;C)
Alt rs80357368(A;A) rs80357368(C;C)
Reference Rs80357368(G;G)
Significance Untested
Disease not specified Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN not specified Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41197765C>G; NC_000017.10:g.41197765C>T
CLNSRC ClinVar
CLNACC RCV000480419.1, RCV000049035.2, RCV000112694.1, RCV000236784.1,