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rs397508989

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508989(-;-)
Make rs397508989(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092888
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508989
ebirs397508989
HLIrs397508989
Exacrs397508989
Varsomers397508989
Maprs397508989
PheGenIrs397508989
hapmaprs397508989
1000 genomesrs397508989
hgdprs397508989
ensemblrs397508989
gopubmedrs397508989
geneviewrs397508989
scholarrs397508989
googlers397508989
pharmgkbrs397508989
gwascentralrs397508989
openSNPrs397508989
23andMers397508989
23andMe allrs397508989
SNP Nexus

SNPshotrs397508989
SNPdbers397508989
MSV3drs397508989
GWAS Ctlgrs397508989
Max Magnitude0
ClinVar
Risk rs397508989(;)
Alt rs397508989(;)
Reference rs397508989(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244905delT
CLNSRC ClinVar
CLNACC RCV000047908.2,