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rs776720591

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs776720591(A;G)
Make rs776720591(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position37755099
GeneTRIOBP
is asnp
is mentioned by
dbSNPrs776720591
dbSNP (classic)rs776720591
ClinGenrs776720591
ebirs776720591
HLIrs776720591
Exacrs776720591
Gnomadrs776720591
Varsomers776720591
LitVarrs776720591
Maprs776720591
PheGenIrs776720591
Biobankrs776720591
1000 genomesrs776720591
hgdprs776720591
ensemblrs776720591
geneviewrs776720591
scholarrs776720591
googlers776720591
pharmgkbrs776720591
gwascentralrs776720591
openSNPrs776720591
23andMers776720591
SNPshotrs776720591
SNPdbers776720591
MSV3drs776720591
GWAS Ctlgrs776720591
Max Magnitude0
ClinVar
Risk rs776720591(G;G)
Alt rs776720591(G;G)
Reference Rs776720591(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRIOBP
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.38151106A>G
CLNSRC
CLNACC RCV000480502.1,