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rs397509305

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397509305(-;-)
Make rs397509305(-;AA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43095848
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509305
ebirs397509305
HLIrs397509305
Exacrs397509305
Varsomers397509305
Maprs397509305
PheGenIrs397509305
hapmaprs397509305
1000 genomesrs397509305
hgdprs397509305
ensemblrs397509305
gopubmedrs397509305
geneviewrs397509305
scholarrs397509305
googlers397509305
pharmgkbrs397509305
gwascentralrs397509305
openSNPrs397509305
23andMers397509305
23andMe allrs397509305
SNP Nexus

SNPshotrs397509305
SNPdbers397509305
MSV3drs397509305
GWAS Ctlgrs397509305
Max Magnitude0
ClinVar
Risk rs397509305(;)
Alt rs397509305(;)
Reference rs397509305(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.41247865_41247866delTT
CLNSRC ClinVar
CLNACC RCV000049083.2,