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

rs397508832

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508832(-;-)
Make rs397508832(-;A)
Make rs397508832(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094450
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508832
ebirs397508832
HLIrs397508832
Exacrs397508832
Varsomers397508832
Maprs397508832
PheGenIrs397508832
hapmaprs397508832
1000 genomesrs397508832
hgdprs397508832
ensemblrs397508832
gopubmedrs397508832
geneviewrs397508832
scholarrs397508832
googlers397508832
pharmgkbrs397508832
gwascentralrs397508832
openSNPrs397508832
23andMers397508832
23andMe allrs397508832
SNP Nexus

SNPshotrs397508832
SNPdbers397508832
MSV3drs397508832
GWAS Ctlgrs397508832
Max Magnitude0
ClinVar
Risk rs397508832(A;A)
Alt rs397508832(A;A)
Reference rs397508832(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246467_41246468insT
CLNSRC ClinVar
CLNACC RCV000047331.2,