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rs397508999

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508999(-;-)
Make rs397508999(-;A)
Make rs397508999(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092841
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508999
ebirs397508999
HLIrs397508999
Exacrs397508999
Varsomers397508999
Maprs397508999
PheGenIrs397508999
hapmaprs397508999
1000 genomesrs397508999
hgdprs397508999
ensemblrs397508999
gopubmedrs397508999
geneviewrs397508999
scholarrs397508999
googlers397508999
pharmgkbrs397508999
gwascentralrs397508999
openSNPrs397508999
23andMers397508999
23andMe allrs397508999
SNP Nexus

SNPshotrs397508999
SNPdbers397508999
MSV3drs397508999
GWAS Ctlgrs397508999
Max Magnitude0
ClinVar
Risk rs397508999(A;A)
Alt rs397508999(A;A)
Reference rs397508999(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244858_41244859insT
CLNSRC ClinVar
CLNACC RCV000047933.2,