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rs746647

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs746647(C;C)
Make rs746647(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31146405
GeneCCHCR1
is asnp
is mentioned by
dbSNPrs746647
ebirs746647
HLIrs746647
Exacrs746647
Varsomers746647
Maprs746647
PheGenIrs746647
hapmaprs746647
1000 genomesrs746647
hgdprs746647
ensemblrs746647
gopubmedrs746647
geneviewrs746647
scholarrs746647
googlers746647
pharmgkbrs746647
gwascentralrs746647
openSNPrs746647
23andMers746647
23andMe allrs746647
SNP Nexus

SNPshotrs746647
SNPdbers746647
MSV3drs746647
GWAS Ctlgrs746647
GMAF0.2392
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 21810746] Genome-wide Association Study Identifies Variations in 6p21.3 Associated With Nevirapine-Induced Rash


[PMID 19143810OA-icon.png] Haplotype-based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1-DQA1-DQB1 haplotype.


ClinVar
Risk rs746647(C;C)
Alt rs746647(C;C)
Reference rs746647(T;T)
Significance Drug-response
Disease nevirapine response - Toxicity/ADR
Variation info
Gene CCHCR1
CLNDBN nevirapine response - Toxicity/ADR
Reversed 1
HGVS NC_000006.11:g.31114182A>G
CLNSRC PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000211168.1,