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rs16879552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16879552(C;T)
Make rs16879552(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position32553698
GeneNRG1
is asnp
is mentioned by
dbSNPrs16879552
ebirs16879552
HLIrs16879552
Exacrs16879552
Varsomers16879552
Maprs16879552
PheGenIrs16879552
hapmaprs16879552
1000 genomesrs16879552
hgdprs16879552
ensemblrs16879552
gopubmedrs16879552
geneviewrs16879552
scholarrs16879552
googlers16879552
pharmgkbrs16879552
gwascentralrs16879552
openSNPrs16879552
23andMers16879552
23andMe allrs16879552
SNP Nexus

SNPshotrs16879552
SNPdbers16879552
MSV3drs16879552
GWAS Ctlgrs16879552
GMAF0.2433
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19196962OA-icon.png] Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.



[PMID 21283760OA-icon.png] Fine mapping of the NRG1 Hirschsprung's disease locus.


GET Evidence
rs16879552
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.174603
summary



[PMID 25475805OA-icon.png] Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease