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rs6904029

From SNPedia

Orientationplus
Stabilizedplus
Make rs6904029(A;A)
Make rs6904029(A;G)
Make rs6904029(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29975290
GeneHCG9
is asnp
is mentioned by
dbSNPrs6904029
ebirs6904029
HLIrs6904029
Exacrs6904029
Varsomers6904029
Maprs6904029
PheGenIrs6904029
hapmaprs6904029
1000 genomesrs6904029
hgdprs6904029
ensemblrs6904029
gopubmedrs6904029
geneviewrs6904029
scholarrs6904029
googlers6904029
pharmgkbrs6904029
gwascentralrs6904029
openSNPrs6904029
23andMers6904029
23andMe allrs6904029
SNP Nexus

SNPshotrs6904029
SNPdbers6904029
MSV3drs6904029
GWAS Ctlgrs6904029
GMAF0.2842
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20410501OA-icon.png]
Trait Vitiligo
Title Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo
Risk Allele A
P-val 1E-21
Odds Ratio 1.49 [1.37-1.61]
OMIM193200
Desc
Variant
Relatedalso
[PMID 22286212OA-icon.png] Genome-Wide Association Study of Classical Hodgkin Lymphoma and Epstein-Barr Virus Status-Defined Subgroups


[PMID 19010793OA-icon.png] Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.


GET Evidence
HCG9-G47R
aa_change Gly47Arg
aa_change_short G47R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.230159
summary



GWAS snp
PMID [PMID 24939585]
Trait Age-related hearing impairment
Title Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.
Risk Allele
P-val 3E-6
Odds Ratio .05 [NR] unit decrease