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rs7835688

From SNPedia

Orientationplus
Stabilizedplus
Make rs7835688(C;C)
Make rs7835688(C;G)
Make rs7835688(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position32553981
GeneNRG1
is asnp
is mentioned by
dbSNPrs7835688
ebirs7835688
HLIrs7835688
Exacrs7835688
Varsomers7835688
Maprs7835688
PheGenIrs7835688
hapmaprs7835688
1000 genomesrs7835688
hgdprs7835688
ensemblrs7835688
gopubmedrs7835688
geneviewrs7835688
scholarrs7835688
googlers7835688
pharmgkbrs7835688
gwascentralrs7835688
openSNPrs7835688
23andMers7835688
23andMe allrs7835688
SNP Nexus

SNPshotrs7835688
SNPdbers7835688
MSV3drs7835688
GWAS Ctlgrs7835688
GMAF0.3352
Max Magnitude
? (C;C) (C;G) (G;G) 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.


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