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rs1800238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1800238(G;T)
Make rs1800238(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position94417738
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs1800238
dbSNP (classic)rs1800238
ClinGenrs1800238
ebirs1800238
HLIrs1800238
Exacrs1800238
Gnomadrs1800238
Varsomers1800238
LitVarrs1800238
Maprs1800238
PheGenIrs1800238
Biobankrs1800238
1000 genomesrs1800238
hgdprs1800238
ensemblrs1800238
geneviewrs1800238
scholarrs1800238
googlers1800238
pharmgkbrs1800238
gwascentralrs1800238
openSNPrs1800238
23andMers1800238
SNPshotrs1800238
SNPdbers1800238
MSV3drs1800238
GWAS Ctlgrs1800238
GMAF0.1143
Max Magnitude0

[PMID 23800505] Associations of Collagen Type I α2 Polymorphisms with the Presence of Intracranial Aneurysms in Patients from Germany


ClinVar
Risk rs1800238(T;T)
Alt rs1800238(T;T)
Reference Rs1800238(G;G)
Significance Non-pathogenic
Disease Osteogenesis Imperfecta Ehlers-Danlos syndrome not specified
Variation info
Gene COL1A2
CLNDBN Osteogenesis Imperfecta, Dominant Ehlers-Danlos syndrome, procollagen proteinase deficient not specified
Reversed 0
HGVS NC_000007.13:g.94047050G>T
CLNSRC
CLNACC RCV000296029.1, RCV000371564.1, RCV000441385.1,



[PMID 29086084] The association between collagen gene polymorphisms and intracranial aneurysms: a meta-analysis.