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rs122467175

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs122467175(C;C)
Make rs122467175(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position49251711
GeneFOXP3
is asnp
is mentioned by
dbSNPrs122467175
ebirs122467175
HLIrs122467175
Exacrs122467175
Varsomers122467175
Maprs122467175
PheGenIrs122467175
hapmaprs122467175
1000 genomesrs122467175
hgdprs122467175
ensemblrs122467175
gopubmedrs122467175
geneviewrs122467175
scholarrs122467175
googlers122467175
pharmgkbrs122467175
gwascentralrs122467175
openSNPrs122467175
23andMers122467175
23andMe allrs122467175
SNP Nexus

SNPshotrs122467175
SNPdbers122467175
MSV3drs122467175
GWAS Ctlgrs122467175
Max Magnitude0
OMIM300292
Desc
Variant0013
Relatedalso
ClinVar
Risk rs122467175(C;C)
Alt rs122467175(C;C)
Reference rs122467175(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.49108172A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012172.11,