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rs10206961

From SNPedia

Orientationplus
Stabilizedplus
Make rs10206961(C;C)
Make rs10206961(C;T)
Make rs10206961(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position85587861
GeneVAMP5
is asnp
is mentioned by
dbSNPrs10206961
dbSNP (old)rs10206961
ClinGenrs10206961
ebirs10206961
HLIrs10206961
Exacrs10206961
Gnomadrs10206961
Varsomers10206961
LitVarrs10206961
Maprs10206961
PheGenIrs10206961
Biobankrs10206961
1000 genomesrs10206961
hgdprs10206961
ensemblrs10206961
gopubmedrs10206961
geneviewrs10206961
scholarrs10206961
googlers10206961
pharmgkbrs10206961
gwascentralrs10206961
openSNPrs10206961
23andMers10206961
23andMe allrs10206961
SNPshotrs10206961
SNPdbers10206961
MSV3drs10206961
GWAS Ctlgrs10206961
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26970437] Potential association of VAMP5 polymorphisms with total colonic aganglionosis in Hirschsprung disease.


[PMID 29695640] Association of VAMP5 and MCC genetic polymorphisms with increased risk of Hirschsprung disease susceptibility in Southern Chinese children.