Disease: Craniosynostosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7528947
rs7528947
Entrez Id: 431704
Gene Symbol: RGS21
RGS21
CUI: C0010278
Disease:
Craniosynostosis 		0.010 GeneticVariation BEFREE For two SNPs in a gene recently associated with bitterant signaling regulation, RGS21, there were no associations with CRS (although the frequency of the minor allele of RGS21, rs7528947, was seen to increase with increasing Lund-Mackay CT staging score). 31137020 2019