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rs397509198

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509198(-;-)
Make rs397509198(-;G)
Make rs397509198(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071077
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509198
ebirs397509198
HLIrs397509198
Exacrs397509198
Varsomers397509198
Maprs397509198
PheGenIrs397509198
hapmaprs397509198
1000 genomesrs397509198
hgdprs397509198
ensemblrs397509198
gopubmedrs397509198
geneviewrs397509198
scholarrs397509198
googlers397509198
pharmgkbrs397509198
gwascentralrs397509198
openSNPrs397509198
23andMers397509198
23andMe allrs397509198
SNP Nexus

SNPshotrs397509198
SNPdbers397509198
MSV3drs397509198
GWAS Ctlgrs397509198
Max Magnitude0
ClinVar
Risk rs397509198(G;G)
Alt rs397509198(G;G)
Reference rs397509198(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41223095dupC
CLNSRC ClinVar
CLNACC RCV000048671.2,