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rs397509015

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs397509015(-;-)
Make rs397509015(-;GT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092696
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509015
ebirs397509015
HLIrs397509015
Exacrs397509015
Varsomers397509015
Maprs397509015
PheGenIrs397509015
hapmaprs397509015
1000 genomesrs397509015
hgdprs397509015
ensemblrs397509015
gopubmedrs397509015
geneviewrs397509015
scholarrs397509015
googlers397509015
pharmgkbrs397509015
gwascentralrs397509015
openSNPrs397509015
23andMers397509015
23andMe allrs397509015
SNP Nexus

SNPshotrs397509015
SNPdbers397509015
MSV3drs397509015
GWAS Ctlgrs397509015
Max Magnitude0
ClinVar
Risk rs397509015(;)
Alt rs397509015(;)
Reference rs397509015(GT;GT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244713_41244714delAC
CLNSRC ClinVar
CLNACC RCV000047983.2,