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rs1064793812

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position61784355
GeneBRIP1
is asnp
is mentioned by
dbSNPrs1064793812
dbSNP (old)rs1064793812
ClinGenrs1064793812
ebirs1064793812
HLIrs1064793812
Exacrs1064793812
Gnomadrs1064793812
Varsomers1064793812
Maprs1064793812
PheGenIrs1064793812
Biobankrs1064793812
1000 genomesrs1064793812
hgdprs1064793812
ensemblrs1064793812
gopubmedrs1064793812
geneviewrs1064793812
scholarrs1064793812
googlers1064793812
pharmgkbrs1064793812
gwascentralrs1064793812
openSNPrs1064793812
23andMers1064793812
23andMe allrs1064793812
SNPshotrs1064793812
SNPdbers1064793812
MSV3drs1064793812
GWAS Ctlgrs1064793812
Max Magnitude0
ClinVar
Risk rs1064793812(-;-)
Alt rs1064793812(-;-)
Reference Rs1064793812(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BRIP1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.59861716delC
CLNSRC
CLNACC RCV000484034.1,