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rs730881457

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;T) 6 BRCA1 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs730881457(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43124052
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs730881457
dbSNP (old)rs730881457
ClinGenrs730881457
ebirs730881457
HLIrs730881457
Exacrs730881457
Gnomadrs730881457
Varsomers730881457
Maprs730881457
PheGenIrs730881457
Biobankrs730881457
1000 genomesrs730881457
hgdprs730881457
ensemblrs730881457
gopubmedrs730881457
geneviewrs730881457
scholarrs730881457
googlers730881457
pharmgkbrs730881457
gwascentralrs730881457
openSNPrs730881457
23andMers730881457
23andMe allrs730881457
SNP Nexus

SNPshotrs730881457
SNPdbers730881457
MSV3drs730881457
GWAS Ctlgrs730881457
Max Magnitude6
ClinVar
Risk rs730881457(-;-)
Alt rs730881457(-;-)
Reference Rs730881457(T;T)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene NBR2 BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41276069delA
CLNSRC
CLNACC RCV000159895.1, RCV000241339.1,