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rs397509318

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509318(G;T)
Make rs397509318(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094744
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509318
ebirs397509318
HLIrs397509318
Exacrs397509318
Varsomers397509318
Maprs397509318
PheGenIrs397509318
hapmaprs397509318
1000 genomesrs397509318
hgdprs397509318
ensemblrs397509318
gopubmedrs397509318
geneviewrs397509318
scholarrs397509318
googlers397509318
pharmgkbrs397509318
gwascentralrs397509318
openSNPrs397509318
23andMers397509318
23andMe allrs397509318
SNP Nexus

SNPshotrs397509318
SNPdbers397509318
MSV3drs397509318
GWAS Ctlgrs397509318
Max Magnitude0
ClinVar
Risk rs397509318(A,T;A,T)
Alt rs397509318(A,T;A,T)
Reference rs397509318(G;G)
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.41246761C>A; NC_000017.10:g.41246761C>T
CLNSRC ClinVar
CLNACC RCV000049131.2, RCV000120297.1,