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rs441051

From SNPedia

Orientationplus
Stabilizedplus
Make rs441051(C;C)
Make rs441051(C;T)
Make rs441051(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position94424688
GeneCHRNA1, COL1A2
is asnp
is mentioned by
dbSNPrs441051
ebirs441051
HLIrs441051
Exacrs441051
Varsomers441051
Maprs441051
PheGenIrs441051
hapmaprs441051
1000 genomesrs441051
hgdprs441051
ensemblrs441051
gopubmedrs441051
geneviewrs441051
scholarrs441051
googlers441051
pharmgkbrs441051
gwascentralrs441051
openSNPrs441051
23andMers441051
23andMe allrs441051
SNP Nexus

SNPshotrs441051
SNPdbers441051
MSV3drs441051
GWAS Ctlgrs441051
GMAF0.1869
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs441051
PubMedID [PMID 17903307OA-icon.png]
Condition Mean forced vital capacity from 2 exams
Gene COL1A2
Risk Allele
pValue 2.00E-006
OR NA
95% CI



[PMID 20140262OA-icon.png] Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth.


GET Evidence
rs441051
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.773438
summary