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rs80358345

From SNPedia

Orientationminus
Geno Mag Summary
(CTG;CTG) 0 common in clinvar
Make rs80358345(-;-)
Make rs80358345(-;GCT)
Make rs80358345(GCT;GCT)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43063947
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358345
ebirs80358345
HLIrs80358345
Exacrs80358345
Varsomers80358345
Maprs80358345
PheGenIrs80358345
hapmaprs80358345
1000 genomesrs80358345
hgdprs80358345
ensemblrs80358345
gopubmedrs80358345
geneviewrs80358345
scholarrs80358345
googlers80358345
pharmgkbrs80358345
gwascentralrs80358345
openSNPrs80358345
23andMers80358345
23andMe allrs80358345
SNP Nexus

SNPshotrs80358345
SNPdbers80358345
MSV3drs80358345
GWAS Ctlgrs80358345
Max Magnitude0
ClinVar
Risk rs80358345(;)
Alt rs80358345(;)
Reference rs80358345(CTG;CTG)
Significance Probable-Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000017.10:g.41215963_41215965delCAG
CLNSRC
CLNACC RCV000048779.2, RCV000083215.3, RCV000166817.1, RCV000237025.1,