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rs397508921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs397508921(-;-)
Make rs397508921(-;TA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093581
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508921
ebirs397508921
HLIrs397508921
Exacrs397508921
Varsomers397508921
Maprs397508921
PheGenIrs397508921
hapmaprs397508921
1000 genomesrs397508921
hgdprs397508921
ensemblrs397508921
gopubmedrs397508921
geneviewrs397508921
scholarrs397508921
googlers397508921
pharmgkbrs397508921
gwascentralrs397508921
openSNPrs397508921
23andMers397508921
23andMe allrs397508921
SNP Nexus

SNPshotrs397508921
SNPdbers397508921
MSV3drs397508921
GWAS Ctlgrs397508921
Max Magnitude0
ClinVar
Risk rs397508921(;)
Alt rs397508921(;)
Reference rs397508921(TA;TA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245598_41245599delTA
CLNSRC ClinVar
CLNACC RCV000047650.2,