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rs1057517590

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517590(-;-)
Make rs1057517590(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43063370
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1057517590
dbSNP (classic)rs1057517590
ClinGenrs1057517590
ebirs1057517590
HLIrs1057517590
Exacrs1057517590
Gnomadrs1057517590
Varsomers1057517590
LitVarrs1057517590
Maprs1057517590
PheGenIrs1057517590
Biobankrs1057517590
1000 genomesrs1057517590
hgdprs1057517590
ensemblrs1057517590
geneviewrs1057517590
scholarrs1057517590
googlers1057517590
pharmgkbrs1057517590
gwascentralrs1057517590
openSNPrs1057517590
23andMers1057517590
SNPshotrs1057517590
SNPdbers1057517590
MSV3drs1057517590
GWAS Ctlgrs1057517590
Max Magnitude0
ClinVar
Risk rs1057517590(-;-)
Alt rs1057517590(-;-)
Reference Rs1057517590(T;T)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41215387delA
CLNSRC
CLNACC RCV000410980.1,