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rs9282834

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9282834(A;A)
Make rs9282834(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position43111408
GeneRET
is asnp
is mentioned by
dbSNPrs9282834
dbSNP (old)rs9282834
ClinGenrs9282834
ebirs9282834
HLIrs9282834
Exacrs9282834
Gnomadrs9282834
Varsomers9282834
Maprs9282834
PheGenIrs9282834
Biobankrs9282834
1000 genomesrs9282834
hgdprs9282834
ensemblrs9282834
gopubmedrs9282834
geneviewrs9282834
scholarrs9282834
googlers9282834
pharmgkbrs9282834
gwascentralrs9282834
openSNPrs9282834
23andMers9282834
23andMe allrs9282834
SNP Nexus

SNPshotrs9282834
SNPdbers9282834
MSV3drs9282834
GWAS Ctlgrs9282834
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 27702942] Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
ClinVar
Risk rs9282834(A;A)
Alt rs9282834(A;A)
Reference Rs9282834(G;G)
Significance Probable-non-pathogenic
Disease not specified Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia Hirschsprung Disease
Variation info
Gene RET
CLNDBN not specified Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia, type 2 Hirschsprung Disease, Dominant
Reversed 0
HGVS NC_000010.10:g.43606856G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000121997.2, RCV000163289.1, RCV000205420.3, RCV000307925.1,