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rs2295418

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2295418(A;A)
Make rs2295418(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position225937685
GeneLEFTY2
is asnp
is mentioned by
dbSNPrs2295418
ebirs2295418
HLIrs2295418
Exacrs2295418
Varsomers2295418
Maprs2295418
PheGenIrs2295418
hapmaprs2295418
1000 genomesrs2295418
hgdprs2295418
ensemblrs2295418
gopubmedrs2295418
geneviewrs2295418
scholarrs2295418
googlers2295418
pharmgkbrs2295418
gwascentralrs2295418
openSNPrs2295418
23andMers2295418
23andMe allrs2295418
SNP Nexus

SNPshotrs2295418
SNPdbers2295418
MSV3drs2295418
GWAS Ctlgrs2295418
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 25111179OA-icon.png] Characterization of Nodal/TGF-Lefty Signaling Pathway Gene Variants for Possible Roles in Congenital Heart Diseases
ClinVar
Risk rs2295418(A;A)
Alt rs2295418(A;A)
Reference rs2295418(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene LEFTY2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.226125385G>A
CLNSRC ClinVar GeneDx
CLNACC RCV000126616.1,