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rs887199

From SNPedia

Orientationplus
Stabilizedplus
Make rs887199(A;A)
Make rs887199(A;G)
Make rs887199(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19974432
GeneARVCF
is asnp
is mentioned by
dbSNPrs887199
ebirs887199
HLIrs887199
Exacrs887199
Varsomers887199
Maprs887199
PheGenIrs887199
hapmaprs887199
1000 genomesrs887199
hgdprs887199
ensemblrs887199
gopubmedrs887199
geneviewrs887199
scholarrs887199
googlers887199
pharmgkbrs887199
gwascentralrs887199
openSNPrs887199
23andMers887199
23andMe allrs887199
SNP Nexus

SNPshotrs887199
SNPdbers887199
MSV3drs887199
GWAS Ctlgrs887199
GMAF0.3416
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19508883] ARVCF single marker and haplotypic association with schizophrenia


[PMID 18574484OA-icon.png] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.