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rs2224391

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2224391(A;C)
Make rs2224391(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position5260703
GeneFARS2, LYRM4
is asnp
is mentioned by
dbSNPrs2224391
dbSNP (old)rs2224391
ClinGenrs2224391
ebirs2224391
HLIrs2224391
Exacrs2224391
Varsomers2224391
Maprs2224391
PheGenIrs2224391
Biobankrs2224391
1000 genomesrs2224391
hgdprs2224391
ensemblrs2224391
gopubmedrs2224391
geneviewrs2224391
scholarrs2224391
googlers2224391
pharmgkbrs2224391
gwascentralrs2224391
openSNPrs2224391
23andMers2224391
23andMe allrs2224391
SNP Nexus

SNPshotrs2224391
SNPdbers2224391
MSV3drs2224391
GWAS Ctlgrs2224391
GMAF0.3926
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21998595OA-icon.png]
Trait
Title Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry.
Risk Allele A
P-val 0.000003
Odds Ratio 0.0490 None

[PMID 21968932] Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia.


GET Evidence
LYRM4-S11A
aa_change Ser11Ala
aa_change_short S11A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.4175
summary



ClinVar
Risk rs2224391(C;C)
Alt rs2224391(C;C)
Reference Rs2224391(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene FARS2 LYRM4
CLNDBN not specified
Reversed 0
HGVS NC_000006.11:g.5260936A>C
CLNSRC
CLNACC RCV000443713.1,