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

rs397508908

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508908(-;-)
Make rs397508908(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093726
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508908
ebirs397508908
HLIrs397508908
Exacrs397508908
Varsomers397508908
Maprs397508908
PheGenIrs397508908
hapmaprs397508908
1000 genomesrs397508908
hgdprs397508908
ensemblrs397508908
gopubmedrs397508908
geneviewrs397508908
scholarrs397508908
googlers397508908
pharmgkbrs397508908
gwascentralrs397508908
openSNPrs397508908
23andMers397508908
23andMe allrs397508908
SNP Nexus

SNPshotrs397508908
SNPdbers397508908
MSV3drs397508908
GWAS Ctlgrs397508908
Max Magnitude0
ClinVar
Risk rs397508908(;)
Alt rs397508908(;)
Reference rs397508908(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245743delT
CLNSRC ClinVar
CLNACC RCV000047591.2,