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rs7988100

From SNPedia

Orientationplus
Stabilizedplus
Make rs7988100(A;A)
Make rs7988100(A;G)
Make rs7988100(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position101227208
GeneNALCN
is asnp
is mentioned by
dbSNPrs7988100
ebirs7988100
HLIrs7988100
Exacrs7988100
Varsomers7988100
Maprs7988100
PheGenIrs7988100
hapmaprs7988100
1000 genomesrs7988100
hgdprs7988100
ensemblrs7988100
gopubmedrs7988100
geneviewrs7988100
scholarrs7988100
googlers7988100
pharmgkbrs7988100
gwascentralrs7988100
openSNPrs7988100
23andMers7988100
23andMe allrs7988100
SNP Nexus

SNPshotrs7988100
SNPdbers7988100
MSV3drs7988100
GWAS Ctlgrs7988100
GMAF0.2149
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM125350
DescFAILURE OF TOOTH ERUPTION, PRIMARY; PFE
Variant
Relatedalso
[PMID 19061984OA-icon.png] PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.