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rs397509223

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ATGC;ATGC) 0 common in clinvar
Make rs397509223(-;-)
Make rs397509223(-;ATGC)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063948
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509223
ebirs397509223
HLIrs397509223
Exacrs397509223
Varsomers397509223
Maprs397509223
PheGenIrs397509223
hapmaprs397509223
1000 genomesrs397509223
hgdprs397509223
ensemblrs397509223
gopubmedrs397509223
geneviewrs397509223
scholarrs397509223
googlers397509223
pharmgkbrs397509223
gwascentralrs397509223
openSNPrs397509223
23andMers397509223
23andMe allrs397509223
SNP Nexus

SNPshotrs397509223
SNPdbers397509223
MSV3drs397509223
GWAS Ctlgrs397509223
Max Magnitude0
ClinVar
Risk rs397509223(;)
Alt rs397509223(;)
Reference rs397509223(ATGC;ATGC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41215965_41215968delGCAT
CLNSRC ClinVar
CLNACC RCV000048777.2,