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rs397508886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508886(-;-)
Make rs397508886(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093961
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508886
ebirs397508886
HLIrs397508886
Exacrs397508886
Varsomers397508886
Maprs397508886
PheGenIrs397508886
hapmaprs397508886
1000 genomesrs397508886
hgdprs397508886
ensemblrs397508886
gopubmedrs397508886
geneviewrs397508886
scholarrs397508886
googlers397508886
pharmgkbrs397508886
gwascentralrs397508886
openSNPrs397508886
23andMers397508886
23andMe allrs397508886
SNP Nexus

SNPshotrs397508886
SNPdbers397508886
MSV3drs397508886
GWAS Ctlgrs397508886
Max Magnitude0
ClinVar
Risk rs397508886(;)
Alt rs397508886(;)
Reference rs397508886(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245978delC
CLNSRC ClinVar
CLNACC RCV000047528.2,