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rs122467174

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs122467174(A;A)
Make rs122467174(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position49258503
GeneFOXP3
is asnp
is mentioned by
dbSNPrs122467174
ebirs122467174
HLIrs122467174
Exacrs122467174
Varsomers122467174
Maprs122467174
PheGenIrs122467174
hapmaprs122467174
1000 genomesrs122467174
hgdprs122467174
ensemblrs122467174
gopubmedrs122467174
geneviewrs122467174
scholarrs122467174
googlers122467174
pharmgkbrs122467174
gwascentralrs122467174
openSNPrs122467174
23andMers122467174
23andMe allrs122467174
SNP Nexus

SNPshotrs122467174
SNPdbers122467174
MSV3drs122467174
GWAS Ctlgrs122467174
Max Magnitude0
OMIM300292
Desc
Variant0012
Relatedalso
ClinVar
Risk rs122467174(A;A)
Alt rs122467174(A;A)
Reference rs122467174(G;G)
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.49114960C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012171.11,