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rs397509235

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509235(-;-)
Make rs397509235(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063344
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509235
ebirs397509235
HLIrs397509235
Exacrs397509235
Varsomers397509235
Maprs397509235
PheGenIrs397509235
hapmaprs397509235
1000 genomesrs397509235
hgdprs397509235
ensemblrs397509235
gopubmedrs397509235
geneviewrs397509235
scholarrs397509235
googlers397509235
pharmgkbrs397509235
gwascentralrs397509235
openSNPrs397509235
23andMers397509235
23andMe allrs397509235
SNP Nexus

SNPshotrs397509235
SNPdbers397509235
MSV3drs397509235
GWAS Ctlgrs397509235
Max Magnitude0
ClinVar
Risk rs397509235(;)
Alt rs397509235(;)
Reference rs397509235(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41215361delT
CLNSRC ClinVar
CLNACC RCV000048846.2,