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rs397509224

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCTG;GCTG) 0 common in clinvar
Make rs397509224(GCTG;TTCATTCTGC)
Make rs397509224(TTCATTCTGC;TTCATTCTGC)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063946
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509224
ebirs397509224
HLIrs397509224
Exacrs397509224
Varsomers397509224
Maprs397509224
PheGenIrs397509224
hapmaprs397509224
1000 genomesrs397509224
hgdprs397509224
ensemblrs397509224
gopubmedrs397509224
geneviewrs397509224
scholarrs397509224
googlers397509224
pharmgkbrs397509224
gwascentralrs397509224
openSNPrs397509224
23andMers397509224
23andMe allrs397509224
SNP Nexus

SNPshotrs397509224
SNPdbers397509224
MSV3drs397509224
GWAS Ctlgrs397509224
Max Magnitude0
ClinVar
Risk rs397509224(TTCATTCTGC;TTCATTCTGC)
Alt rs397509224(TTCATTCTGC;TTCATTCTGC)
Reference rs397509224(GCTG;GCTG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41215963_41215966delCAGCinsGCAGAATGAA
CLNSRC ClinVar
CLNACC RCV000048778.2,