rs121917720

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121917720(C;T)

Make rs121917720(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

36663031

Gene	LOC105370455, PAX9

is a	snp
is	mentioned by
dbSNP	rs121917720
dbSNP (classic)	rs121917720
ClinGen	rs121917720
ebi	rs121917720
HLI	rs121917720
Exac	rs121917720
Gnomad	rs121917720
Varsome	rs121917720
LitVar	rs121917720
Map	rs121917720
PheGenI	rs121917720
Biobank	rs121917720
1000 genomes	rs121917720
hgdp	rs121917720
ensembl	rs121917720
geneview	rs121917720
scholar	rs121917720
google	rs121917720
pharmgkb	rs121917720
gwascentral	rs121917720
openSNP	rs121917720
23andMe	rs121917720
SNPshot	rs121917720
SNPdbe	rs121917720
MSV3d	rs121917720
GWAS Ctlg	rs121917720

Max Magnitude

0

ClinVar
Risk	rs121917720(T;T)
Alt	rs121917720(T;T)
Reference	Rs121917720(C;C)
Significance	Pathogenic
Disease	Tooth agenesis
Variation	info
Gene	PAX9
CLNDBN	Tooth agenesis, selective, 3
Reversed	0
HGVS	NC_000014.8:g.37132236C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014791.27,