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rs397509311

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs397509311(-;-)
Make rs397509311(-;TC)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124024
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs397509311
ebirs397509311
HLIrs397509311
Exacrs397509311
Varsomers397509311
Maprs397509311
PheGenIrs397509311
hapmaprs397509311
1000 genomesrs397509311
hgdprs397509311
ensemblrs397509311
gopubmedrs397509311
geneviewrs397509311
scholarrs397509311
googlers397509311
pharmgkbrs397509311
gwascentralrs397509311
openSNPrs397509311
23andMers397509311
23andMe allrs397509311
SNP Nexus

SNPshotrs397509311
SNPdbers397509311
MSV3drs397509311
GWAS Ctlgrs397509311
Max Magnitude0
ClinVar
Risk rs397509311(;)
Alt rs397509311(;)
Reference rs397509311(TC;TC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene NBR2 BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41276041_41276042delGA
CLNSRC ClinVar
CLNACC RCV000049110.2,