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rs397509227

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509227(A;G)
Make rs397509227(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063928
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509227
ebirs397509227
HLIrs397509227
Exacrs397509227
Varsomers397509227
Maprs397509227
PheGenIrs397509227
hapmaprs397509227
1000 genomesrs397509227
hgdprs397509227
ensemblrs397509227
gopubmedrs397509227
geneviewrs397509227
scholarrs397509227
googlers397509227
pharmgkbrs397509227
gwascentralrs397509227
openSNPrs397509227
23andMers397509227
23andMe allrs397509227
SNP Nexus

SNPshotrs397509227
SNPdbers397509227
MSV3drs397509227
GWAS Ctlgrs397509227
Max Magnitude0
ClinVar
Risk rs397509227(G;G)
Alt rs397509227(G;G)
Reference rs397509227(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.41215945T>C
CLNSRC ClinVar
CLNACC RCV000048793.2,