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rs397509272

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTGTGGTGAAGGAGCTT;CTGTGGTGAAGGAGCTT) 0 common in clinvar
Make rs397509272(-;-)
Make rs397509272(-;CTGTGGTGAAGGAGCTT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049142
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509272
ebirs397509272
HLIrs397509272
Exacrs397509272
Varsomers397509272
Maprs397509272
PheGenIrs397509272
hapmaprs397509272
1000 genomesrs397509272
hgdprs397509272
ensemblrs397509272
gopubmedrs397509272
geneviewrs397509272
scholarrs397509272
googlers397509272
pharmgkbrs397509272
gwascentralrs397509272
openSNPrs397509272
23andMers397509272
23andMe allrs397509272
SNP Nexus

SNPshotrs397509272
SNPdbers397509272
MSV3drs397509272
GWAS Ctlgrs397509272
Max Magnitude0
ClinVar
Risk rs397509272(;)
Alt rs397509272(;)
Reference rs397509272(CTGTGGTGAAGGAGCTT;CTGTGGTGAAGGAGCTT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41201159_41201175del17
CLNSRC ClinVar
CLNACC RCV000048964.2,