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rs1064794890

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome17
Position61857194
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1064794890
dbSNP (old)rs1064794890
ClinGenrs1064794890
ebirs1064794890
HLIrs1064794890
Exacrs1064794890
Gnomadrs1064794890
Varsomers1064794890
LitVarrs1064794890
Maprs1064794890
PheGenIrs1064794890
Biobankrs1064794890
1000 genomesrs1064794890
hgdprs1064794890
ensemblrs1064794890
gopubmedrs1064794890
geneviewrs1064794890
scholarrs1064794890
googlers1064794890
pharmgkbrs1064794890
gwascentralrs1064794890
openSNPrs1064794890
23andMers1064794890
23andMe allrs1064794890
SNPshotrs1064794890
SNPdbers1064794890
MSV3drs1064794890
GWAS Ctlgrs1064794890
Max Magnitude0
ClinVar
Risk rs1064794890(-;-)
Alt rs1064794890(-;-)
Reference Rs1064794890(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59934555delT
CLNSRC
CLNACC RCV000484917.1,