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rs397509060

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTAAT;TTAAT) 0 common in clinvar
Make rs397509060(-;-)
Make rs397509060(-;TTAAT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092168
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509060
ebirs397509060
HLIrs397509060
Exacrs397509060
Varsomers397509060
Maprs397509060
PheGenIrs397509060
hapmaprs397509060
1000 genomesrs397509060
hgdprs397509060
ensemblrs397509060
gopubmedrs397509060
geneviewrs397509060
scholarrs397509060
googlers397509060
pharmgkbrs397509060
gwascentralrs397509060
openSNPrs397509060
23andMers397509060
23andMe allrs397509060
SNP Nexus

SNPshotrs397509060
SNPdbers397509060
MSV3drs397509060
GWAS Ctlgrs397509060
Max Magnitude0
ClinVar
Risk rs397509060(;)
Alt rs397509060(;)
Reference rs397509060(TTAAT;TTAAT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244185_41244189delATTAA
CLNSRC ClinVar
CLNACC RCV000048165.2,