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rs397508879

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGAGA;GGAGA) 0 common in clinvar
Make rs397508879(-;-)
Make rs397508879(-;GGAGA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094010
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508879
ebirs397508879
HLIrs397508879
Exacrs397508879
Varsomers397508879
Maprs397508879
PheGenIrs397508879
hapmaprs397508879
1000 genomesrs397508879
hgdprs397508879
ensemblrs397508879
gopubmedrs397508879
geneviewrs397508879
scholarrs397508879
googlers397508879
pharmgkbrs397508879
gwascentralrs397508879
openSNPrs397508879
23andMers397508879
23andMe allrs397508879
SNP Nexus

SNPshotrs397508879
SNPdbers397508879
MSV3drs397508879
GWAS Ctlgrs397508879
Max Magnitude0
ClinVar
Risk rs397508879(;)
Alt rs397508879(;)
Reference rs397508879(GGAGA;GGAGA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246027_41246031delTCTCC
CLNSRC ClinVar
CLNACC RCV000047511.2,