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rs142426358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs142426358(C;C)
Make rs142426358(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position37814375
GeneGDNF
is asnp
is mentioned by
dbSNPrs142426358
dbSNP (old)rs142426358
ClinGenrs142426358
ebirs142426358
HLIrs142426358
Exacrs142426358
Gnomadrs142426358
Varsomers142426358
Maprs142426358
PheGenIrs142426358
Biobankrs142426358
1000 genomesrs142426358
hgdprs142426358
ensemblrs142426358
gopubmedrs142426358
geneviewrs142426358
scholarrs142426358
googlers142426358
pharmgkbrs142426358
gwascentralrs142426358
openSNPrs142426358
23andMers142426358
23andMe allrs142426358
SNP Nexus

SNPshotrs142426358
SNPdbers142426358
MSV3drs142426358
GWAS Ctlgrs142426358
Max Magnitude0

[PMID 24997227] New alterations at potentially regulated regions of the Glial Derived Neurotrophic Factor gene in bipolar disorder

ClinVar
Risk rs142426358(C;C)
Alt rs142426358(C;C)
Reference Rs142426358(T;T)
Significance Probable-non-pathogenic
Disease Hirschsprung Disease
Variation info
Gene GDNF
CLNDBN Hirschsprung Disease, Dominant
Reversed 0
HGVS NC_000005.9:g.37814477T>C
CLNSRC
CLNACC RCV000326850.1,