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rs397509319

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509319(C;C)
Make rs397509319(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094743
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509319
ebirs397509319
HLIrs397509319
Exacrs397509319
Varsomers397509319
Maprs397509319
PheGenIrs397509319
hapmaprs397509319
1000 genomesrs397509319
hgdprs397509319
ensemblrs397509319
gopubmedrs397509319
geneviewrs397509319
scholarrs397509319
googlers397509319
pharmgkbrs397509319
gwascentralrs397509319
openSNPrs397509319
23andMers397509319
23andMe allrs397509319
SNP Nexus

SNPshotrs397509319
SNPdbers397509319
MSV3drs397509319
GWAS Ctlgrs397509319
Max Magnitude0
ClinVar
Risk rs397509319(A,C,T;A,C,T)
Alt rs397509319(A,C,T;A,C,T)
Reference rs397509319(G;G)
Significance Untested
Disease Familial cancer of breast not specified Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast not specified Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41246760C>A; NC_000017.10:g.41246760C>G; NC_000017.10:g.41246760C>T
CLNSRC ClinVar
CLNACC RCV000049133.2, RCV000049132.2, RCV000159945.1, RCV000165328.1,