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rs6984045

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6984045(C;C)
Make rs6984045(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position130080167
GeneASAP1
is asnp
is mentioned by
dbSNPrs6984045
ebirs6984045
HLIrs6984045
Exacrs6984045
Varsomers6984045
Maprs6984045
PheGenIrs6984045
hapmaprs6984045
1000 genomesrs6984045
hgdprs6984045
ensemblrs6984045
gopubmedrs6984045
geneviewrs6984045
scholarrs6984045
googlers6984045
pharmgkbrs6984045
gwascentralrs6984045
openSNPrs6984045
23andMers6984045
23andMe allrs6984045
SNP Nexus

SNPshotrs6984045
SNPdbers6984045
MSV3drs6984045
GWAS Ctlgrs6984045
GMAF0.02388
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19525955]
Trait Multiple sclerosis
Title Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
Risk Allele C
P-val 0.000002
Odds Ratio 1.59 [NR]


GET Evidence
rs6984045
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.015873
summary