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rs122467173

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs122467173(C;C)
Make rs122467173(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position49253200
GeneFOXP3
is asnp
is mentioned by
dbSNPrs122467173
ebirs122467173
HLIrs122467173
Exacrs122467173
Varsomers122467173
Maprs122467173
PheGenIrs122467173
hapmaprs122467173
1000 genomesrs122467173
hgdprs122467173
ensemblrs122467173
gopubmedrs122467173
geneviewrs122467173
scholarrs122467173
googlers122467173
pharmgkbrs122467173
gwascentralrs122467173
openSNPrs122467173
23andMers122467173
23andMe allrs122467173
SNP Nexus

SNPshotrs122467173
SNPdbers122467173
MSV3drs122467173
GWAS Ctlgrs122467173
Max Magnitude0
OMIM300292
Desc
Variant0010
Relatedalso
ClinVar
Risk rs122467173(C;C)
Alt rs122467173(C;C)
Reference rs122467173(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.49109661A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012169.11,