Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607042

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607042(A;A)
Make rs267607042(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position44951942
GeneSETBP1
is asnp
is mentioned by
dbSNPrs267607042
ebirs267607042
HLIrs267607042
Exacrs267607042
Varsomers267607042
Maprs267607042
PheGenIrs267607042
hapmaprs267607042
1000 genomesrs267607042
hgdprs267607042
ensemblrs267607042
gopubmedrs267607042
geneviewrs267607042
scholarrs267607042
googlers267607042
pharmgkbrs267607042
gwascentralrs267607042
openSNPrs267607042
23andMers267607042
23andMe allrs267607042
SNP Nexus

SNPshotrs267607042
SNPdbers267607042
MSV3drs267607042
GWAS Ctlgrs267607042
Max Magnitude0
ClinVar
Risk rs267607042(A,C;A,C)
Alt rs267607042(A,C;A,C)
Reference rs267607042(G;G)
Significance Pathogenic
Disease Schinzel-Giedion syndrome
Variation info
Gene SETBP1
CLNDBN Schinzel-Giedion syndrome
Reversed 0
HGVS NC_000018.9:g.42531907G>A; NC_000018.9:g.42531907G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001087.3, RCV000147458.1,