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rs397509185

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397509185(-;-)
Make rs397509185(-;AG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43099864
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509185
ebirs397509185
HLIrs397509185
Exacrs397509185
Varsomers397509185
Maprs397509185
PheGenIrs397509185
hapmaprs397509185
1000 genomesrs397509185
hgdprs397509185
ensemblrs397509185
gopubmedrs397509185
geneviewrs397509185
scholarrs397509185
googlers397509185
pharmgkbrs397509185
gwascentralrs397509185
openSNPrs397509185
23andMers397509185
23andMe allrs397509185
SNP Nexus

SNPshotrs397509185
SNPdbers397509185
MSV3drs397509185
GWAS Ctlgrs397509185
Max Magnitude0
ClinVar
Risk rs397509185(;)
Alt rs397509185(;)
Reference rs397509185(AG;AG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41251881_41251882delCT
CLNSRC ClinVar
CLNACC RCV000048599.2,