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rs122467171

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs122467171(-;-)
Make rs122467171(-;GGA)
Make rs122467171(GGA;GGA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position49255493
GeneFOXP3
is asnp
is mentioned by
dbSNPrs122467171
ebirs122467171
HLIrs122467171
Exacrs122467171
Varsomers122467171
Maprs122467171
PheGenIrs122467171
hapmaprs122467171
1000 genomesrs122467171
hgdprs122467171
ensemblrs122467171
gopubmedrs122467171
geneviewrs122467171
scholarrs122467171
googlers122467171
pharmgkbrs122467171
gwascentralrs122467171
openSNPrs122467171
23andMers122467171
23andMe allrs122467171
SNP Nexus

SNPshotrs122467171
SNPdbers122467171
MSV3drs122467171
GWAS Ctlgrs122467171
Max Magnitude0
OMIM300292
Desc
Variant0007
Relatedalso
ClinVar
Risk rs122467171(;)
Alt rs122467171(;)
Reference rs122467171(GAG;GAG)
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.49111954_49111956delTCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000012166.11,