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rs1064795413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position61799128
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1064795413
dbSNP (old)rs1064795413
ClinGenrs1064795413
ebirs1064795413
HLIrs1064795413
Exacrs1064795413
Gnomadrs1064795413
Varsomers1064795413
LitVarrs1064795413
Maprs1064795413
PheGenIrs1064795413
Biobankrs1064795413
1000 genomesrs1064795413
hgdprs1064795413
ensemblrs1064795413
gopubmedrs1064795413
geneviewrs1064795413
scholarrs1064795413
googlers1064795413
pharmgkbrs1064795413
gwascentralrs1064795413
openSNPrs1064795413
23andMers1064795413
23andMe allrs1064795413
SNPshotrs1064795413
SNPdbers1064795413
MSV3drs1064795413
GWAS Ctlgrs1064795413
Max Magnitude0
ClinVar
Risk rs1064795413(-;-)
Alt rs1064795413(-;-)
Reference Rs1064795413(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59876489delG
CLNSRC
CLNACC RCV000479813.1,