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rs16999349

From SNPedia

Orientationplus
Stabilizedplus
Make rs16999349(A;A)
Make rs16999349(A;G)
Make rs16999349(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position48536386
GeneFAM19A5
is asnp
is mentioned by
dbSNPrs16999349
ebirs16999349
HLIrs16999349
Exacrs16999349
Varsomers16999349
Maprs16999349
PheGenIrs16999349
hapmaprs16999349
1000 genomesrs16999349
hgdprs16999349
ensemblrs16999349
gopubmedrs16999349
geneviewrs16999349
scholarrs16999349
googlers16999349
pharmgkbrs16999349
gwascentralrs16999349
openSNPrs16999349
23andMers16999349
23andMe allrs16999349
SNP Nexus

SNPshotrs16999349
SNPdbers16999349
MSV3drs16999349
GWAS Ctlgrs16999349
GMAF0.1194
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs16999349
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.210938
summary