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rs397509341

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397509341(-;-)
Make rs397509341(-;AA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094545
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509341
ebirs397509341
HLIrs397509341
Exacrs397509341
Varsomers397509341
Maprs397509341
PheGenIrs397509341
hapmaprs397509341
1000 genomesrs397509341
hgdprs397509341
ensemblrs397509341
gopubmedrs397509341
geneviewrs397509341
scholarrs397509341
googlers397509341
pharmgkbrs397509341
gwascentralrs397509341
openSNPrs397509341
23andMers397509341
23andMe allrs397509341
SNP Nexus

SNPshotrs397509341
SNPdbers397509341
MSV3drs397509341
GWAS Ctlgrs397509341
Max Magnitude0
ClinVar
Risk rs397509341(;)
Alt rs397509341(;)
Reference rs397509341(AA;AA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246562_41246563delTT
CLNSRC ClinVar
CLNACC RCV000049212.2,