Have questions? Visit https://www.reddit.com/r/SNPedia

rs80357007

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80357007(G;T)
Make rs80357007(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051107
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357007
ebirs80357007
HLIrs80357007
Exacrs80357007
Varsomers80357007
Maprs80357007
PheGenIrs80357007
hapmaprs80357007
1000 genomesrs80357007
hgdprs80357007
ensemblrs80357007
gopubmedrs80357007
geneviewrs80357007
scholarrs80357007
googlers80357007
pharmgkbrs80357007
gwascentralrs80357007
openSNPrs80357007
23andMers80357007
23andMe allrs80357007
SNP Nexus

SNPshotrs80357007
SNPdbers80357007
MSV3drs80357007
GWAS Ctlgrs80357007
Max Magnitude0
ClinVar
Risk rs80357007(T;T)
Alt rs80357007(T;T)
Reference rs80357007(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 not provided
Reversed 1
HGVS NC_000017.10:g.41203124C>A
CLNSRC ClinVar
CLNACC RCV000048910.4, RCV000112603.1, RCV000212199.1,