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rs7992226

From SNPedia

Orientationplus
Stabilizedplus
Make rs7992226(A;A)
Make rs7992226(A;G)
Make rs7992226(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position101145489
GeneNALCN
is asnp
is mentioned by
dbSNPrs7992226
ebirs7992226
HLIrs7992226
Exacrs7992226
Varsomers7992226
Maprs7992226
PheGenIrs7992226
hapmaprs7992226
1000 genomesrs7992226
hgdprs7992226
ensemblrs7992226
gopubmedrs7992226
geneviewrs7992226
scholarrs7992226
googlers7992226
pharmgkbrs7992226
gwascentralrs7992226
openSNPrs7992226
23andMers7992226
23andMe allrs7992226
SNP Nexus

SNPshotrs7992226
SNPdbers7992226
MSV3drs7992226
GWAS Ctlgrs7992226
GMAF0.1938
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs7992226
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.179688
summary