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

rs397508910

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508910(-;-)
Make rs397508910(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093714
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508910
ebirs397508910
HLIrs397508910
Exacrs397508910
Varsomers397508910
Maprs397508910
PheGenIrs397508910
hapmaprs397508910
1000 genomesrs397508910
hgdprs397508910
ensemblrs397508910
gopubmedrs397508910
geneviewrs397508910
scholarrs397508910
googlers397508910
pharmgkbrs397508910
gwascentralrs397508910
openSNPrs397508910
23andMers397508910
23andMe allrs397508910
SNP Nexus

SNPshotrs397508910
SNPdbers397508910
MSV3drs397508910
GWAS Ctlgrs397508910
Max Magnitude0
ClinVar
Risk rs397508910(;)
Alt rs397508910(;)
Reference rs397508910(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.41245731delG
CLNSRC ClinVar
CLNACC RCV000047593.2,