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rs397509246

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509246(A;A)
Make rs397509246(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43057071
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509246
ebirs397509246
HLIrs397509246
Exacrs397509246
Varsomers397509246
Maprs397509246
PheGenIrs397509246
hapmaprs397509246
1000 genomesrs397509246
hgdprs397509246
ensemblrs397509246
gopubmedrs397509246
geneviewrs397509246
scholarrs397509246
googlers397509246
pharmgkbrs397509246
gwascentralrs397509246
openSNPrs397509246
23andMers397509246
23andMe allrs397509246
SNP Nexus

SNPshotrs397509246
SNPdbers397509246
MSV3drs397509246
GWAS Ctlgrs397509246
Max Magnitude0
ClinVar
Risk rs397509246(A,C;A,C)
Alt rs397509246(A,C;A,C)
Reference rs397509246(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41209088C>G; NC_000017.10:g.41209088C>T
CLNSRC ClinVar
CLNACC RCV000048890.2, RCV000048889.2,