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rs1064794689

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position61743062
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1064794689
dbSNP (old)rs1064794689
ClinGenrs1064794689
ebirs1064794689
HLIrs1064794689
Exacrs1064794689
Gnomadrs1064794689
Varsomers1064794689
Maprs1064794689
PheGenIrs1064794689
Biobankrs1064794689
1000 genomesrs1064794689
hgdprs1064794689
ensemblrs1064794689
gopubmedrs1064794689
geneviewrs1064794689
scholarrs1064794689
googlers1064794689
pharmgkbrs1064794689
gwascentralrs1064794689
openSNPrs1064794689
23andMers1064794689
23andMe allrs1064794689
SNPshotrs1064794689
SNPdbers1064794689
MSV3drs1064794689
GWAS Ctlgrs1064794689
Max Magnitude0
ClinVar
Risk rs1064794689(-;-)
Alt rs1064794689(-;-)
Reference Rs1064794689(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59820423delC
CLNSRC
CLNACC RCV000477985.1,