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rs397509333

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509333(-;-)
Make rs397509333(-;C)
Make rs397509333(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094627
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509333
ebirs397509333
HLIrs397509333
Exacrs397509333
Varsomers397509333
Maprs397509333
PheGenIrs397509333
hapmaprs397509333
1000 genomesrs397509333
hgdprs397509333
ensemblrs397509333
gopubmedrs397509333
geneviewrs397509333
scholarrs397509333
googlers397509333
pharmgkbrs397509333
gwascentralrs397509333
openSNPrs397509333
23andMers397509333
23andMe allrs397509333
SNP Nexus

SNPshotrs397509333
SNPdbers397509333
MSV3drs397509333
GWAS Ctlgrs397509333
Max Magnitude0
ClinVar
Risk rs397509333(C;C)
Alt rs397509333(C;C)
Reference rs397509333(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246644_41246645insG
CLNSRC ClinVar
CLNACC RCV000049183.2,