Have questions? Visit https://www.reddit.com/r/SNPedia

rs2817419

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2817419(A;A)
Make rs2817419(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position50845193
GeneTFAP2B
is asnp
is mentioned by
dbSNPrs2817419
dbSNP (old)rs2817419
ClinGenrs2817419
ebirs2817419
HLIrs2817419
Exacrs2817419
Gnomadrs2817419
Varsomers2817419
Maprs2817419
PheGenIrs2817419
Biobankrs2817419
1000 genomesrs2817419
hgdprs2817419
ensemblrs2817419
gopubmedrs2817419
geneviewrs2817419
scholarrs2817419
googlers2817419
pharmgkbrs2817419
gwascentralrs2817419
openSNPrs2817419
23andMers2817419
23andMe allrs2817419
SNP Nexus

SNPshotrs2817419
SNPdbers2817419
MSV3drs2817419
GWAS Ctlgrs2817419
GMAF0.2443
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20581741OA-icon.png] Patterns of gene expression in the ductus arteriosus are related to environmental and genetic risk factors for persistent ductus patency


ClinVar
Risk rs2817419(A;A)
Alt rs2817419(A;A)
Reference Rs2817419(G;G)
Significance Non-pathogenic
Disease Char syndrome
Variation info
Gene TFAP2B
CLNDBN Char syndrome
Reversed 0
HGVS NC_000006.11:g.50812906G>A
CLNSRC
CLNACC RCV000317760.1,