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rs397509020

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509020(-;-)
Make rs397509020(-;A)
Make rs397509020(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092660
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509020
ebirs397509020
HLIrs397509020
Exacrs397509020
Varsomers397509020
Maprs397509020
PheGenIrs397509020
hapmaprs397509020
1000 genomesrs397509020
hgdprs397509020
ensemblrs397509020
gopubmedrs397509020
geneviewrs397509020
scholarrs397509020
googlers397509020
pharmgkbrs397509020
gwascentralrs397509020
openSNPrs397509020
23andMers397509020
23andMe allrs397509020
SNP Nexus

SNPshotrs397509020
SNPdbers397509020
MSV3drs397509020
GWAS Ctlgrs397509020
Max Magnitude0
ClinVar
Risk rs397509020(A;A)
Alt rs397509020(A;A)
Reference rs397509020(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244678dupT
CLNSRC ClinVar
CLNACC RCV000047996.2,