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rs1064793059

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Chromosome17
Position43045737
GeneBRCA1
is asnp
is mentioned by
dbSNPrs1064793059
dbSNP (classic)rs1064793059
ClinGenrs1064793059
ebirs1064793059
HLIrs1064793059
Exacrs1064793059
Gnomadrs1064793059
Varsomers1064793059
LitVarrs1064793059
Maprs1064793059
PheGenIrs1064793059
Biobankrs1064793059
1000 genomesrs1064793059
hgdprs1064793059
ensemblrs1064793059
geneviewrs1064793059
scholarrs1064793059
googlers1064793059
pharmgkbrs1064793059
gwascentralrs1064793059
openSNPrs1064793059
23andMers1064793059
SNPshotrs1064793059
SNPdbers1064793059
MSV3drs1064793059
GWAS Ctlgrs1064793059
Max Magnitude0
ClinVar
Risk rs1064793059(-;-)
Alt rs1064793059(-;-)
Reference Rs1064793059(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.41197754_41197755delAG
CLNSRC
CLNACC RCV000479128.1,