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rs6896969

From SNPedia

Orientationplus
Stabilizedplus
Make rs6896969(A;A)
Make rs6896969(A;C)
Make rs6896969(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position40424324
is asnp
is mentioned by
dbSNPrs6896969
ebirs6896969
HLIrs6896969
Exacrs6896969
Varsomers6896969
Maprs6896969
PheGenIrs6896969
hapmaprs6896969
1000 genomesrs6896969
hgdprs6896969
ensemblrs6896969
gopubmedrs6896969
geneviewrs6896969
scholarrs6896969
googlers6896969
pharmgkbrs6896969
gwascentralrs6896969
openSNPrs6896969
23andMers6896969
23andMe allrs6896969
SNP Nexus

SNPshotrs6896969
SNPdbers6896969
MSV3drs6896969
GWAS Ctlgrs6896969
GMAF0.4601
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19525953OA-icon.png]
Trait Multiple sclerosis
Title Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
Risk Allele C
P-val 2E-7
Odds Ratio 1.10 [1.01-1.20]


GET Evidence
rs6896969
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5625
summary



[PMID 26538147OA-icon.png] PTGER4 gene variant rs76523431 is a candidate risk factor for radiological joint damage in rheumatoid arthritis patients: a genetic study of six cohorts