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rs397508855

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508855(-;-)
Make rs397508855(-;G)
Make rs397508855(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094191
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508855
ebirs397508855
HLIrs397508855
Exacrs397508855
Varsomers397508855
Maprs397508855
PheGenIrs397508855
hapmaprs397508855
1000 genomesrs397508855
hgdprs397508855
ensemblrs397508855
gopubmedrs397508855
geneviewrs397508855
scholarrs397508855
googlers397508855
pharmgkbrs397508855
gwascentralrs397508855
openSNPrs397508855
23andMers397508855
23andMe allrs397508855
SNP Nexus

SNPshotrs397508855
SNPdbers397508855
MSV3drs397508855
GWAS Ctlgrs397508855
Max Magnitude0
ClinVar
Risk rs397508855(G;G)
Alt rs397508855(G;G)
Reference rs397508855(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246209dupC
CLNSRC ClinVar
CLNACC RCV000047424.2,