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rs397508847

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508847(-;-)
Make rs397508847(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43115738
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508847
ebirs397508847
HLIrs397508847
Exacrs397508847
Varsomers397508847
Maprs397508847
PheGenIrs397508847
hapmaprs397508847
1000 genomesrs397508847
hgdprs397508847
ensemblrs397508847
gopubmedrs397508847
geneviewrs397508847
scholarrs397508847
googlers397508847
pharmgkbrs397508847
gwascentralrs397508847
openSNPrs397508847
23andMers397508847
23andMe allrs397508847
SNP Nexus

SNPshotrs397508847
SNPdbers397508847
MSV3drs397508847
GWAS Ctlgrs397508847
Max Magnitude0
ClinVar
Risk rs397508847(;)
Alt rs397508847(;)
Reference rs397508847(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.41267755delT
CLNSRC ClinVar
CLNACC RCV000047384.2,