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rs397509099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs397509099(-;-)
Make rs397509099(-;GT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091774
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509099
ebirs397509099
HLIrs397509099
Exacrs397509099
Varsomers397509099
Maprs397509099
PheGenIrs397509099
hapmaprs397509099
1000 genomesrs397509099
hgdprs397509099
ensemblrs397509099
gopubmedrs397509099
geneviewrs397509099
scholarrs397509099
googlers397509099
pharmgkbrs397509099
gwascentralrs397509099
openSNPrs397509099
23andMers397509099
23andMe allrs397509099
SNP Nexus

SNPshotrs397509099
SNPdbers397509099
MSV3drs397509099
GWAS Ctlgrs397509099
Max Magnitude0
ClinVar
Risk rs397509099(;)
Alt rs397509099(;)
Reference rs397509099(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.41243791_41243792delAC
CLNSRC ClinVar
CLNACC RCV000048313.2,