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rs11884776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11884776(C;T)
Make rs11884776(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position73519796
GeneALMS1
is asnp
is mentioned by
dbSNPrs11884776
dbSNP (old)rs11884776
ClinGenrs11884776
ebirs11884776
HLIrs11884776
Exacrs11884776
Varsomers11884776
Maprs11884776
PheGenIrs11884776
Biobankrs11884776
1000 genomesrs11884776
hgdprs11884776
ensemblrs11884776
gopubmedrs11884776
geneviewrs11884776
scholarrs11884776
googlers11884776
pharmgkbrs11884776
gwascentralrs11884776
openSNPrs11884776
23andMers11884776
23andMe allrs11884776
SNP Nexus

SNPshotrs11884776
SNPdbers11884776
MSV3drs11884776
GWAS Ctlgrs11884776
Max Magnitude0
GWAS snp
PMID [PMID 24586186OA-icon.png]
Trait Urinary metabolites (H-NMR features)
Title Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links.
Risk Allele C
P-val 6E-17
Odds Ratio .35 [NR] unit increase


ClinVar
Risk rs11884776(T;T)
Alt rs11884776(T;T)
Reference Rs11884776(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ALMS1
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.73746923C>T
CLNSRC
CLNACC RCV000440420.1,