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rs397509314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509314(-;-)
Make rs397509314(-;A)
Make rs397509314(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094788
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509314
ebirs397509314
HLIrs397509314
Exacrs397509314
Varsomers397509314
Maprs397509314
PheGenIrs397509314
hapmaprs397509314
1000 genomesrs397509314
hgdprs397509314
ensemblrs397509314
gopubmedrs397509314
geneviewrs397509314
scholarrs397509314
googlers397509314
pharmgkbrs397509314
gwascentralrs397509314
openSNPrs397509314
23andMers397509314
23andMe allrs397509314
SNP Nexus

SNPshotrs397509314
SNPdbers397509314
MSV3drs397509314
GWAS Ctlgrs397509314
Max Magnitude0
ClinVar
Risk rs397509314(A;A)
Alt rs397509314(A;A)
Reference rs397509314(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246806dupT
CLNSRC ClinVar
CLNACC RCV000049117.2,