Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508868

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508868(-;-)
Make rs397508868(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094139
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508868
ebirs397508868
HLIrs397508868
Exacrs397508868
Varsomers397508868
Maprs397508868
PheGenIrs397508868
hapmaprs397508868
1000 genomesrs397508868
hgdprs397508868
ensemblrs397508868
gopubmedrs397508868
geneviewrs397508868
scholarrs397508868
googlers397508868
pharmgkbrs397508868
gwascentralrs397508868
openSNPrs397508868
23andMers397508868
23andMe allrs397508868
SNP Nexus

SNPshotrs397508868
SNPdbers397508868
MSV3drs397508868
GWAS Ctlgrs397508868
Max Magnitude0
ClinVar
Risk rs397508868(;)
Alt rs397508868(;)
Reference rs397508868(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246156delG
CLNSRC ClinVar
CLNACC RCV000047459.2,