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rs2229207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2229207(C;C)
Make rs2229207(C;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position33241945
GeneIFNAR2
is asnp
is mentioned by
dbSNPrs2229207
ebirs2229207
HLIrs2229207
Exacrs2229207
Varsomers2229207
Maprs2229207
PheGenIrs2229207
hapmaprs2229207
1000 genomesrs2229207
hgdprs2229207
ensemblrs2229207
gopubmedrs2229207
geneviewrs2229207
scholarrs2229207
googlers2229207
pharmgkbrs2229207
gwascentralrs2229207
openSNPrs2229207
23andMers2229207
23andMe allrs2229207
SNP Nexus

SNPshotrs2229207
SNPdbers2229207
MSV3drs2229207
GWAS Ctlgrs2229207
GMAF0.118
Max Magnitude0
OMIM602376
Desc
Variant0001
Relatedalso
? (C;C) (C;T) (T;T)


ClinVar
Risk rs2229207(C;C)
Alt rs2229207(C;C)
Reference rs2229207(T;T)
Significance Other
Disease Hepatitis b virus
Variation info
Gene IFNAR2
CLNDBN Hepatitis b virus, susceptibility to
Reversed 0
HGVS NC_000021.8:g.34614250T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007711.2,



[PMID 19434718OA-icon.png] Variants in interferon-alpha pathway genes and response to pegylated interferon-Alpha2a plus ribavirin for treatment of chronic hepatitis C virus infection in the hepatitis C antiviral long-term treatment against cirrhosis trial.


GET Evidence
IFNAR2-F8S
aa_change Phe8Ser
aa_change_short F8S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0764083
summary