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rs397508863

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508863(-;-)
Make rs397508863(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094151
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508863
ebirs397508863
HLIrs397508863
Exacrs397508863
Varsomers397508863
Maprs397508863
PheGenIrs397508863
hapmaprs397508863
1000 genomesrs397508863
hgdprs397508863
ensemblrs397508863
gopubmedrs397508863
geneviewrs397508863
scholarrs397508863
googlers397508863
pharmgkbrs397508863
gwascentralrs397508863
openSNPrs397508863
23andMers397508863
23andMe allrs397508863
SNP Nexus

SNPshotrs397508863
SNPdbers397508863
MSV3drs397508863
GWAS Ctlgrs397508863
Max Magnitude0
ClinVar
Risk rs397508863(;)
Alt rs397508863(;)
Reference rs397508863(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.41246168delT
CLNSRC ClinVar
CLNACC RCV000047446.2,