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rs2505535

From SNPedia

Orientationminus
Stabilizedminus
Make rs2505535(C;C)
Make rs2505535(C;T)
Make rs2505535(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position43097595
GeneRET
is asnp
is mentioned by
dbSNPrs2505535
ebirs2505535
HLIrs2505535
Exacrs2505535
Varsomers2505535
Maprs2505535
PheGenIrs2505535
hapmaprs2505535
1000 genomesrs2505535
hgdprs2505535
ensemblrs2505535
gopubmedrs2505535
geneviewrs2505535
scholarrs2505535
googlers2505535
pharmgkbrs2505535
gwascentralrs2505535
openSNPrs2505535
23andMers2505535
23andMe allrs2505535
SNP Nexus

SNPshotrs2505535
SNPdbers2505535
MSV3drs2505535
GWAS Ctlgrs2505535
GMAF0.2576
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 18612588] the C allele of rs2505535 would appear to represent a protecting allele for the Chinese population


[PMID 15759212OA-icon.png] Identifying candidate Hirschsprung disease-associated RET variants.


[PMID 20532249OA-icon.png] Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.