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rs397509172

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509172(A;A)
Make rs397509172(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43104121
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509172
ebirs397509172
HLIrs397509172
Exacrs397509172
Varsomers397509172
Maprs397509172
PheGenIrs397509172
hapmaprs397509172
1000 genomesrs397509172
hgdprs397509172
ensemblrs397509172
gopubmedrs397509172
geneviewrs397509172
scholarrs397509172
googlers397509172
pharmgkbrs397509172
gwascentralrs397509172
openSNPrs397509172
23andMers397509172
23andMe allrs397509172
SNP Nexus

SNPshotrs397509172
SNPdbers397509172
MSV3drs397509172
GWAS Ctlgrs397509172
Max Magnitude0
ClinVar
Risk rs397509172(A;A)
Alt rs397509172(A;A)
Reference rs397509172(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41256138C>T
CLNSRC ClinVar
CLNACC RCV000048555.2,