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rs397508883

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCAG;GCAG) 0 common in clinvar
Make rs397508883(GCAG;TAAA)
Make rs397508883(TAAA;TAAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093967
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508883
ebirs397508883
HLIrs397508883
Exacrs397508883
Varsomers397508883
Maprs397508883
PheGenIrs397508883
hapmaprs397508883
1000 genomesrs397508883
hgdprs397508883
ensemblrs397508883
gopubmedrs397508883
geneviewrs397508883
scholarrs397508883
googlers397508883
pharmgkbrs397508883
gwascentralrs397508883
openSNPrs397508883
23andMers397508883
23andMe allrs397508883
SNP Nexus

SNPshotrs397508883
SNPdbers397508883
MSV3drs397508883
GWAS Ctlgrs397508883
Max Magnitude0
ClinVar
Risk rs397508883(TAAA;TAAA)
Alt rs397508883(TAAA;TAAA)
Reference rs397508883(GCAG;GCAG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245984_41245987delCTGCinsTTTA
CLNSRC ClinVar
CLNACC RCV000047524.2,