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rs397509181

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509181(-;-)
Make rs397509181(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43076487
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509181
ebirs397509181
HLIrs397509181
Exacrs397509181
Varsomers397509181
Maprs397509181
PheGenIrs397509181
hapmaprs397509181
1000 genomesrs397509181
hgdprs397509181
ensemblrs397509181
gopubmedrs397509181
geneviewrs397509181
scholarrs397509181
googlers397509181
pharmgkbrs397509181
gwascentralrs397509181
openSNPrs397509181
23andMers397509181
23andMe allrs397509181
SNP Nexus

SNPshotrs397509181
SNPdbers397509181
MSV3drs397509181
GWAS Ctlgrs397509181
Max Magnitude0
ClinVar
Risk rs397509181(;)
Alt rs397509181(;)
Reference rs397509181(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41228504delC
CLNSRC ClinVar
CLNACC RCV000048573.2,