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rs397508920

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAGTGAAGAG;CAGTGAAGAG) 0 common in clinvar
Make rs397508920(-;-)
Make rs397508920(-;CAGTGAAGAG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093584
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508920
ebirs397508920
HLIrs397508920
Exacrs397508920
Varsomers397508920
Maprs397508920
PheGenIrs397508920
hapmaprs397508920
1000 genomesrs397508920
hgdprs397508920
ensemblrs397508920
gopubmedrs397508920
geneviewrs397508920
scholarrs397508920
googlers397508920
pharmgkbrs397508920
gwascentralrs397508920
openSNPrs397508920
23andMers397508920
23andMe allrs397508920
SNP Nexus

SNPshotrs397508920
SNPdbers397508920
MSV3drs397508920
GWAS Ctlgrs397508920
Max Magnitude0
ClinVar
Risk rs397508920(;)
Alt rs397508920(;)
Reference rs397508920(CAGTGAAGAG;CAGTGAAGAG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245601_41245610delCTCTTCACTG
CLNSRC ClinVar
CLNACC RCV000047647.2,