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rs147805077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147805077(A;A)
Make rs147805077(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position44869229
GeneSETBP1
is asnp
is mentioned by
dbSNPrs147805077
dbSNP (old)rs147805077
ClinGenrs147805077
ebirs147805077
HLIrs147805077
Exacrs147805077
Gnomadrs147805077
Varsomers147805077
LitVarrs147805077
Maprs147805077
PheGenIrs147805077
Biobankrs147805077
1000 genomesrs147805077
hgdprs147805077
ensemblrs147805077
gopubmedrs147805077
geneviewrs147805077
scholarrs147805077
googlers147805077
pharmgkbrs147805077
gwascentralrs147805077
openSNPrs147805077
23andMers147805077
23andMe allrs147805077
SNPshotrs147805077
SNPdbers147805077
MSV3drs147805077
GWAS Ctlgrs147805077
Max Magnitude0
ClinVar
Risk rs147805077(A;A)
Alt rs147805077(A;A)
Reference Rs147805077(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SETBP1
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.42449194G>A
CLNSRC
CLNACC RCV000494550.1,