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rs80357149

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80357149(C;C)
Make rs80357149(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43047702
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357149
ebirs80357149
HLIrs80357149
Exacrs80357149
Varsomers80357149
Maprs80357149
PheGenIrs80357149
hapmaprs80357149
1000 genomesrs80357149
hgdprs80357149
ensemblrs80357149
gopubmedrs80357149
geneviewrs80357149
scholarrs80357149
googlers80357149
pharmgkbrs80357149
gwascentralrs80357149
openSNPrs80357149
23andMers80357149
23andMe allrs80357149
SNP Nexus

SNPshotrs80357149
SNPdbers80357149
MSV3drs80357149
GWAS Ctlgrs80357149
Max Magnitude0
ClinVar
Risk rs80357149(C;C)
Alt rs80357149(C;C)
Reference rs80357149(G;G)
Significance Untested
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41199719C>G
CLNSRC ClinVar
CLNACC RCV000031249.4, RCV000048981.2,