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rs397509317

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509317(A;A)
Make rs397509317(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094745
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509317
ebirs397509317
HLIrs397509317
Exacrs397509317
Varsomers397509317
Maprs397509317
PheGenIrs397509317
hapmaprs397509317
1000 genomesrs397509317
hgdprs397509317
ensemblrs397509317
gopubmedrs397509317
geneviewrs397509317
scholarrs397509317
googlers397509317
pharmgkbrs397509317
gwascentralrs397509317
openSNPrs397509317
23andMers397509317
23andMe allrs397509317
SNP Nexus

SNPshotrs397509317
SNPdbers397509317
MSV3drs397509317
GWAS Ctlgrs397509317
Max Magnitude0
ClinVar
Risk rs397509317(A;A)
Alt rs397509317(A;A)
Reference rs397509317(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.41246762C>T
CLNSRC ClinVar
CLNACC RCV000049130.2,