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rs397509177

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509177(-;-)
Make rs397509177(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43076525
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509177
ebirs397509177
HLIrs397509177
Exacrs397509177
Varsomers397509177
Maprs397509177
PheGenIrs397509177
hapmaprs397509177
1000 genomesrs397509177
hgdprs397509177
ensemblrs397509177
gopubmedrs397509177
geneviewrs397509177
scholarrs397509177
googlers397509177
pharmgkbrs397509177
gwascentralrs397509177
openSNPrs397509177
23andMers397509177
23andMe allrs397509177
SNP Nexus

SNPshotrs397509177
SNPdbers397509177
MSV3drs397509177
GWAS Ctlgrs397509177
Max Magnitude0
ClinVar
Risk rs397509177(;)
Alt rs397509177(;)
Reference rs397509177(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41228542delT
CLNSRC ClinVar
CLNACC RCV000048560.2,