Have questions? Visit https://www.reddit.com/r/SNPedia

rs122467169

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs122467169(G;G)
Make rs122467169(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position49251698
GeneFOXP3
is asnp
is mentioned by
dbSNPrs122467169
ebirs122467169
HLIrs122467169
Exacrs122467169
Varsomers122467169
Maprs122467169
PheGenIrs122467169
hapmaprs122467169
1000 genomesrs122467169
hgdprs122467169
ensemblrs122467169
gopubmedrs122467169
geneviewrs122467169
scholarrs122467169
googlers122467169
pharmgkbrs122467169
gwascentralrs122467169
openSNPrs122467169
23andMers122467169
23andMe allrs122467169
SNP Nexus

SNPshotrs122467169
SNPdbers122467169
MSV3drs122467169
GWAS Ctlgrs122467169
Max Magnitude0
OMIM300292
Desc
Variant0003
Relatedalso
ClinVar
Risk rs122467169(G;G)
Alt rs122467169(G;G)
Reference rs122467169(T;T)
Significance Pathogenic
Disease Insulin-dependent diabetes mellitus secretory diarrhea syndrome
Variation info
Gene FOXP3
CLNDBN Insulin-dependent diabetes mellitus secretory diarrhea syndrome
Reversed 1
HGVS NC_000023.10:g.49108159A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012162.11,