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rs1064793887

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position61743135
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1064793887
dbSNP (classic)rs1064793887
ClinGenrs1064793887
ebirs1064793887
HLIrs1064793887
Exacrs1064793887
Gnomadrs1064793887
Varsomers1064793887
LitVarrs1064793887
Maprs1064793887
PheGenIrs1064793887
Biobankrs1064793887
1000 genomesrs1064793887
hgdprs1064793887
ensemblrs1064793887
geneviewrs1064793887
scholarrs1064793887
googlers1064793887
pharmgkbrs1064793887
gwascentralrs1064793887
openSNPrs1064793887
23andMers1064793887
23andMe allrs1064793887
SNPshotrs1064793887
SNPdbers1064793887
MSV3drs1064793887
GWAS Ctlgrs1064793887
Max Magnitude0
ClinVar
Risk rs1064793887(A;A)
Alt rs1064793887(A;A)
Reference Rs1064793887(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59820496C>T
CLNSRC
CLNACC RCV000477981.1,