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rs16999684

From SNPedia

Orientationplus
Stabilizedplus
Make rs16999684(A;A)
Make rs16999684(A;C)
Make rs16999684(C;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position48671066
GeneFAM19A5
is asnp
is mentioned by
dbSNPrs16999684
ebirs16999684
HLIrs16999684
Exacrs16999684
Varsomers16999684
Maprs16999684
PheGenIrs16999684
hapmaprs16999684
1000 genomesrs16999684
hgdprs16999684
ensemblrs16999684
gopubmedrs16999684
geneviewrs16999684
scholarrs16999684
googlers16999684
pharmgkbrs16999684
gwascentralrs16999684
openSNPrs16999684
23andMers16999684
23andMe allrs16999684
SNP Nexus

SNPshotrs16999684
SNPdbers16999684
MSV3drs16999684
GWAS Ctlgrs16999684
GMAF0.32
Max Magnitude
? (A;A) (A;C) (C;C) 28


GET Evidence
rs16999684
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.335938
summary