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rs397508827

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397508827(-;-)
Make rs397508827(-;CT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094491
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508827
ebirs397508827
HLIrs397508827
Exacrs397508827
Varsomers397508827
Maprs397508827
PheGenIrs397508827
hapmaprs397508827
1000 genomesrs397508827
hgdprs397508827
ensemblrs397508827
gopubmedrs397508827
geneviewrs397508827
scholarrs397508827
googlers397508827
pharmgkbrs397508827
gwascentralrs397508827
openSNPrs397508827
23andMers397508827
23andMe allrs397508827
SNP Nexus

SNPshotrs397508827
SNPdbers397508827
MSV3drs397508827
GWAS Ctlgrs397508827
Max Magnitude0
ClinVar
Risk rs397508827(;)
Alt rs397508827(;)
Reference rs397508827(CT;CT)
Significance Pathogenic
Disease Familial cancer of breast not provided
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast not provided
Reversed 1
HGVS NC_000017.10:g.41246508_41246509delAG
CLNSRC ClinVar
CLNACC RCV000047316.2, RCV000235412.1,