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rs397508860

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508860(-;-)
Make rs397508860(-;GA)
Make rs397508860(GA;GA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094167
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508860
ebirs397508860
HLIrs397508860
Exacrs397508860
Varsomers397508860
Maprs397508860
PheGenIrs397508860
hapmaprs397508860
1000 genomesrs397508860
hgdprs397508860
ensemblrs397508860
gopubmedrs397508860
geneviewrs397508860
scholarrs397508860
googlers397508860
pharmgkbrs397508860
gwascentralrs397508860
openSNPrs397508860
23andMers397508860
23andMe allrs397508860
SNP Nexus

SNPshotrs397508860
SNPdbers397508860
MSV3drs397508860
GWAS Ctlgrs397508860
Max Magnitude0
ClinVar
Risk rs397508860(GA;GA)
Alt rs397508860(GA;GA)
Reference rs397508860(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246184_41246185insTC
CLNSRC ClinVar
CLNACC RCV000047442.2,