rs7988100

Orientation

plus

Stabilized

plus

Make rs7988100(A;A)

Make rs7988100(A;G)

Make rs7988100(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

101227208

Gene

NALCN

is a	snp
is	mentioned by
dbSNP	rs7988100
dbSNP (classic)	rs7988100
ClinGen	rs7988100
ebi	rs7988100
HLI	rs7988100
Exac	rs7988100
Gnomad	rs7988100
Varsome	rs7988100
LitVar	rs7988100
Map	rs7988100
PheGenI	rs7988100
Biobank	rs7988100
1000 genomes	rs7988100
hgdp	rs7988100
ensembl	rs7988100
geneview	rs7988100
scholar	rs7988100
google	rs7988100
pharmgkb	rs7988100
gwascentral	rs7988100
openSNP	rs7988100
23andMe	rs7988100
SNPshot	rs7988100
SNPdbe	rs7988100
MSV3d	rs7988100
GWAS Ctlg	rs7988100

GMAF

0.2149

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

OMIM	125350
Desc	FAILURE OF TOOTH ERUPTION, PRIMARY; PFE
Variant
Related	also

[PMID 19061984] PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.