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rs397509021

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTCAG;TTCAG) 0 common in clinvar
Make rs397509021(-;-)
Make rs397509021(-;TTCAG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092655
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509021
ebirs397509021
HLIrs397509021
Exacrs397509021
Varsomers397509021
Maprs397509021
PheGenIrs397509021
hapmaprs397509021
1000 genomesrs397509021
hgdprs397509021
ensemblrs397509021
gopubmedrs397509021
geneviewrs397509021
scholarrs397509021
googlers397509021
pharmgkbrs397509021
gwascentralrs397509021
openSNPrs397509021
23andMers397509021
23andMe allrs397509021
SNP Nexus

SNPshotrs397509021
SNPdbers397509021
MSV3drs397509021
GWAS Ctlgrs397509021
Max Magnitude0
ClinVar
Risk rs397509021(;)
Alt rs397509021(;)
Reference rs397509021(TTCAG;TTCAG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244672_41244676delCTGAA
CLNSRC ClinVar
CLNACC RCV000047998.2,