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rs397509162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509162(-;-)
Make rs397509162(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43104132
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509162
ebirs397509162
HLIrs397509162
Exacrs397509162
Varsomers397509162
Maprs397509162
PheGenIrs397509162
hapmaprs397509162
1000 genomesrs397509162
hgdprs397509162
ensemblrs397509162
gopubmedrs397509162
geneviewrs397509162
scholarrs397509162
googlers397509162
pharmgkbrs397509162
gwascentralrs397509162
openSNPrs397509162
23andMers397509162
23andMe allrs397509162
SNP Nexus

SNPshotrs397509162
SNPdbers397509162
MSV3drs397509162
GWAS Ctlgrs397509162
Max Magnitude0
ClinVar
Risk rs397509162(;)
Alt rs397509162(;)
Reference rs397509162(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.41256149delT
CLNSRC ClinVar
CLNACC RCV000048520.2,