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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
dbSNP (classic)rs7992226
ClinGenrs7992226
ebirs7992226
HLIrs7992226
Exacrs7992226
Gnomadrs7992226
Varsomers7992226
LitVarrs7992226
Maprs7992226
PheGenIrs7992226
Biobankrs7992226
1000 genomesrs7992226
hgdprs7992226
ensemblrs7992226
geneviewrs7992226
scholarrs7992226
googlers7992226
pharmgkbrs7992226
gwascentralrs7992226
openSNPrs7992226
23andMers7992226
SNPshotrs7992226
SNPdbers7992226
MSV3drs7992226
GWAS Ctlgrs7992226
GMAF0.1938
Max Magnitude0
? (A;A) (A;G) (G;G) 28