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rs397509118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509118(-;-)
Make rs397509118(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091617
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509118
ebirs397509118
HLIrs397509118
Exacrs397509118
Varsomers397509118
Maprs397509118
PheGenIrs397509118
hapmaprs397509118
1000 genomesrs397509118
hgdprs397509118
ensemblrs397509118
gopubmedrs397509118
geneviewrs397509118
scholarrs397509118
googlers397509118
pharmgkbrs397509118
gwascentralrs397509118
openSNPrs397509118
23andMers397509118
23andMe allrs397509118
SNP Nexus

SNPshotrs397509118
SNPdbers397509118
MSV3drs397509118
GWAS Ctlgrs397509118
Max Magnitude0
ClinVar
Risk rs397509118(;)
Alt rs397509118(;)
Reference rs397509118(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243634delT
CLNSRC ClinVar
CLNACC RCV000048378.2,