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rs397509157

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509157(G;G)
Make rs397509157(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082508
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509157
ebirs397509157
HLIrs397509157
Exacrs397509157
Varsomers397509157
Maprs397509157
PheGenIrs397509157
hapmaprs397509157
1000 genomesrs397509157
hgdprs397509157
ensemblrs397509157
gopubmedrs397509157
geneviewrs397509157
scholarrs397509157
googlers397509157
pharmgkbrs397509157
gwascentralrs397509157
openSNPrs397509157
23andMers397509157
23andMe allrs397509157
SNP Nexus

SNPshotrs397509157
SNPdbers397509157
MSV3drs397509157
GWAS Ctlgrs397509157
Max Magnitude0
ClinVar
Risk rs397509157(G;G)
Alt rs397509157(G;G)
Reference rs397509157(T;T)
Significance Untested
Disease Familial cancer of breast not specified
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast not specified
Reversed 1
HGVS NC_000017.10:g.41234525A>C; NC_000017.10:g.41234525A>G
CLNSRC ClinVar
CLNACC RCV000048502.2, RCV000237031.1,