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rs1057518636

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518636(-;T)
Make rs1057518636(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43047646
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1057518636
dbSNP (old)rs1057518636
ClinGenrs1057518636
ebirs1057518636
HLIrs1057518636
Exacrs1057518636
Gnomadrs1057518636
Varsomers1057518636
Maprs1057518636
PheGenIrs1057518636
Biobankrs1057518636
1000 genomesrs1057518636
hgdprs1057518636
ensemblrs1057518636
gopubmedrs1057518636
geneviewrs1057518636
scholarrs1057518636
googlers1057518636
pharmgkbrs1057518636
gwascentralrs1057518636
openSNPrs1057518636
23andMers1057518636
23andMe allrs1057518636
SNPshotrs1057518636
SNPdbers1057518636
MSV3drs1057518636
GWAS Ctlgrs1057518636
Max Magnitude0
ClinVar
Risk rs1057518636(T;T)
Alt rs1057518636(T;T)
Reference Rs1057518636(-;-)
Significance Pathogenic
Disease Neoplasm of breast
Variation info
Gene BRCA1
CLNDBN Neoplasm of breast
Reversed 1
HGVS NC_000017.10:g.41199663_41199664insA
CLNSRC
CLNACC RCV000413916.1,