Have questions? Visit https://www.reddit.com/r/SNPedia

rs3099844

From SNPedia

Orientationplus
Stabilizedplus
Make rs3099844(A;A)
Make rs3099844(A;C)
Make rs3099844(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31481199
GeneLOC102725068
is asnp
is mentioned by
dbSNPrs3099844
dbSNP (classic)rs3099844
ClinGenrs3099844
ebirs3099844
HLIrs3099844
Exacrs3099844
Gnomadrs3099844
Varsomers3099844
LitVarrs3099844
Maprs3099844
PheGenIrs3099844
Biobankrs3099844
1000 genomesrs3099844
hgdprs3099844
ensemblrs3099844
geneviewrs3099844
scholarrs3099844
googlers3099844
pharmgkbrs3099844
gwascentralrs3099844
openSNPrs3099844
23andMers3099844
SNPshotrs3099844
SNPdbers3099844
MSV3drs3099844
GWAS Ctlgrs3099844
GMAF0.0854
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 19944697] Genome-wide association analysis in primary sclerosing cholangitis


[PMID 20662065OA-icon.png] Genome-wide association study of cardiac manifestations of neonatal lupus identifies candidate loci at 6p21 and 21q22

GWAS snp
PMID [PMID 22399527OA-icon.png]
Trait
Title Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.
Risk Allele A
P-val 2E-8
Odds Ratio 0.1500 None


[PMID 18204098] Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.


[PMID 18309376OA-icon.png] Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus.


[PMID 19197363OA-icon.png] A genome-wide investigation of SNPs and CNVs in schizophrenia.


[PMID 19853236OA-icon.png] Sequence variants in three loci influence monocyte counts and erythrocyte volume.


[PMID 20017995OA-icon.png] A principal-components-based clustering method to identify multiple variants associated with rheumatoid arthritis and arthritis-related autoantibodies.


[PMID 20437058OA-icon.png] The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer.


[PMID 24322967] HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons Syndrome/Toxic Epidermal Necrolysis susceptibility in a population from Mozambique


[PMID 30882006OA-icon.png] STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren's Syndrome: Association with Disease Susceptibility and Clinical Aspects.