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rs1064794668

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome17
Position61684072
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1064794668
dbSNP (old)rs1064794668
ClinGenrs1064794668
ebirs1064794668
HLIrs1064794668
Exacrs1064794668
Gnomadrs1064794668
Varsomers1064794668
Maprs1064794668
PheGenIrs1064794668
Biobankrs1064794668
1000 genomesrs1064794668
hgdprs1064794668
ensemblrs1064794668
gopubmedrs1064794668
geneviewrs1064794668
scholarrs1064794668
googlers1064794668
pharmgkbrs1064794668
gwascentralrs1064794668
openSNPrs1064794668
23andMers1064794668
23andMe allrs1064794668
SNPshotrs1064794668
SNPdbers1064794668
MSV3drs1064794668
GWAS Ctlgrs1064794668
Max Magnitude0
ClinVar
Risk rs1064794668(-;-)
Alt rs1064794668(-;-)
Reference Rs1064794668(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59761433delT
CLNSRC
CLNACC RCV000480248.1,