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rs137941190

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137941190(C;T)
Make rs137941190(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position126345546
GeneDCPS, ST3GAL4-AS1
is asnp
is mentioned by
dbSNPrs137941190
dbSNP (classic)rs137941190
ClinGenrs137941190
ebirs137941190
HLIrs137941190
Exacrs137941190
Gnomadrs137941190
Varsomers137941190
LitVarrs137941190
Maprs137941190
PheGenIrs137941190
Biobankrs137941190
1000 genomesrs137941190
hgdprs137941190
ensemblrs137941190
geneviewrs137941190
scholarrs137941190
googlers137941190
pharmgkbrs137941190
gwascentralrs137941190
openSNPrs137941190
23andMers137941190
SNPshotrs137941190
SNPdbers137941190
MSV3drs137941190
GWAS Ctlgrs137941190
Max Magnitude0
ClinVar
Risk rs137941190(G;G) rs137941190(T;T)
Alt rs137941190(G;G) rs137941190(T;T)
Reference Rs137941190(C;C)
Significance Pathogenic
Disease AL-RAQAD SYNDROME
Variation info
Gene ST3GAL4-AS1 DCPS
CLNDBN AL-RAQAD SYNDROME
Reversed 0
HGVS NC_000011.9:g.126215441C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000412619.1,