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

rs2294021

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2294021(C;C)
Make rs2294021(C;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position49249149
GeneCCDC22
is asnp
is mentioned by
dbSNPrs2294021
dbSNP (old)rs2294021
ClinGenrs2294021
ebirs2294021
HLIrs2294021
Exacrs2294021
Gnomadrs2294021
Varsomers2294021
Maprs2294021
PheGenIrs2294021
Biobankrs2294021
1000 genomesrs2294021
hgdprs2294021
ensemblrs2294021
gopubmedrs2294021
geneviewrs2294021
scholarrs2294021
googlers2294021
pharmgkbrs2294021
gwascentralrs2294021
openSNPrs2294021
23andMers2294021
23andMe allrs2294021
SNP Nexus

SNPshotrs2294021
SNPdbers2294021
MSV3drs2294021
GWAS Ctlgrs2294021
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 25499308] The transcription factor Forkhead Box P3 gene variants affect idiopathic recurrent pregnancy loss


[PMID 28253599] [Association of ulcerative colitis with fork head/winged helix transcription factor-3 gene polymorphisms in Chinese patients].


ClinVar
Risk rs2294021(C;C)
Alt rs2294021(C;C)
Reference Rs2294021(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CCDC22
CLNDBN not specified
Reversed 0
HGVS NC_000023.10:g.49105610T>C
CLNSRC
CLNACC RCV000353781.1,