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rs1057519558

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519558(G;T)
Make rs1057519558(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43082518
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1057519558
dbSNP (old)rs1057519558
ClinGenrs1057519558
ebirs1057519558
HLIrs1057519558
Exacrs1057519558
Gnomadrs1057519558
Varsomers1057519558
LitVarrs1057519558
Maprs1057519558
PheGenIrs1057519558
Biobankrs1057519558
1000 genomesrs1057519558
hgdprs1057519558
ensemblrs1057519558
gopubmedrs1057519558
geneviewrs1057519558
scholarrs1057519558
googlers1057519558
pharmgkbrs1057519558
gwascentralrs1057519558
openSNPrs1057519558
23andMers1057519558
23andMe allrs1057519558
SNPshotrs1057519558
SNPdbers1057519558
MSV3drs1057519558
GWAS Ctlgrs1057519558
Max Magnitude0
ClinVar
Risk rs1057519558(T;T)
Alt rs1057519558(T;T)
Reference Rs1057519558(G;G)
Significance Probable-Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41234535C>A
CLNSRC
CLNACC RCV000417027.1,