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rs1064795649

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Chromosome17
Position61799205
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1064795649
dbSNP (old)rs1064795649
ClinGenrs1064795649
ebirs1064795649
HLIrs1064795649
Exacrs1064795649
Gnomadrs1064795649
Varsomers1064795649
Maprs1064795649
PheGenIrs1064795649
Biobankrs1064795649
1000 genomesrs1064795649
hgdprs1064795649
ensemblrs1064795649
gopubmedrs1064795649
geneviewrs1064795649
scholarrs1064795649
googlers1064795649
pharmgkbrs1064795649
gwascentralrs1064795649
openSNPrs1064795649
23andMers1064795649
23andMe allrs1064795649
SNPshotrs1064795649
SNPdbers1064795649
MSV3drs1064795649
GWAS Ctlgrs1064795649
Max Magnitude0
ClinVar
Risk rs1064795649(-;-)
Alt rs1064795649(-;-)
Reference Rs1064795649(GA;GA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59876566_59876567delTC
CLNSRC
CLNACC RCV000479248.1,