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rs397509329

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509329(-;-)
Make rs397509329(-;T)
Make rs397509329(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094703
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509329
ebirs397509329
HLIrs397509329
Exacrs397509329
Varsomers397509329
Maprs397509329
PheGenIrs397509329
hapmaprs397509329
1000 genomesrs397509329
hgdprs397509329
ensemblrs397509329
gopubmedrs397509329
geneviewrs397509329
scholarrs397509329
googlers397509329
pharmgkbrs397509329
gwascentralrs397509329
openSNPrs397509329
23andMers397509329
23andMe allrs397509329
SNP Nexus

SNPshotrs397509329
SNPdbers397509329
MSV3drs397509329
GWAS Ctlgrs397509329
Max Magnitude0
ClinVar
Risk rs397509329(T;T)
Alt rs397509329(T;T)
Reference rs397509329(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246720_41246721insA
CLNSRC ClinVar
CLNACC RCV000049162.2,