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

rs387906564

From SNPedia

Merged intors80357571
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906564(-;-)
Make rs387906564(-;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position43091906
GeneBRCA1
is asnp
is mentioned by
dbSNPrs387906564
dbSNP (old)rs387906564
ClinGenrs387906564
ebirs387906564
HLIrs387906564
Exacrs387906564
Gnomadrs387906564
Varsomers387906564
Maprs387906564
PheGenIrs387906564
Biobankrs387906564
1000 genomesrs387906564
hgdprs387906564
ensemblrs387906564
gopubmedrs387906564
geneviewrs387906564
scholarrs387906564
googlers387906564
pharmgkbrs387906564
gwascentralrs387906564
openSNPrs387906564
23andMers387906564
23andMe allrs387906564
SNP Nexus

SNPshotrs387906564
SNPdbers387906564
MSV3drs387906564
GWAS Ctlgrs387906564
StatusMerged into rs80357571
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs387906564(T;T)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41243922delA
CLNSRC Breast Cancer Information Core (BRCA1) OMIM Allelic Variant
CLNACC RCV000048261.2, RCV000112140.5,