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

rs80358154

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80358154(A;G)
Make rs80358154(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43097240
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358154
ebirs80358154
HLIrs80358154
Exacrs80358154
Varsomers80358154
Maprs80358154
PheGenIrs80358154
hapmaprs80358154
1000 genomesrs80358154
hgdprs80358154
ensemblrs80358154
gopubmedrs80358154
geneviewrs80358154
scholarrs80358154
googlers80358154
pharmgkbrs80358154
gwascentralrs80358154
openSNPrs80358154
23andMers80358154
23andMe allrs80358154
SNP Nexus

SNPshotrs80358154
SNPdbers80358154
MSV3drs80358154
GWAS Ctlgrs80358154
Max Magnitude0
ClinVar
Risk rs80358154(G;G)
Alt rs80358154(G;G)
Reference rs80358154(A;A)
Significance Probable-non-pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations not specified
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Tumor susceptibility linked to germline BAP1 mutations not specified
Reversed 1
HGVS NC_000017.10:g.41249257T>C
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000049066.2, RCV000112748.1, RCV000217340.1, RCV000237043.1,