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rs1064793626

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position61780307
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1064793626
dbSNP (old)rs1064793626
ClinGenrs1064793626
ebirs1064793626
HLIrs1064793626
Exacrs1064793626
Gnomadrs1064793626
Varsomers1064793626
LitVarrs1064793626
Maprs1064793626
PheGenIrs1064793626
Biobankrs1064793626
1000 genomesrs1064793626
hgdprs1064793626
ensemblrs1064793626
gopubmedrs1064793626
geneviewrs1064793626
scholarrs1064793626
googlers1064793626
pharmgkbrs1064793626
gwascentralrs1064793626
openSNPrs1064793626
23andMers1064793626
23andMe allrs1064793626
SNPshotrs1064793626
SNPdbers1064793626
MSV3drs1064793626
GWAS Ctlgrs1064793626
Max Magnitude0
ClinVar
Risk rs1064793626(-;-)
Alt rs1064793626(-;-)
Reference Rs1064793626(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59857668delG
CLNSRC
CLNACC RCV000487110.1,