rs28933971

Orientation

plus

Stabilized

plus

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

Make rs28933971(C;C)

Make rs28933971(C;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

36662975

Gene	LOC105370455, PAX9

is a	snp
is	mentioned by
dbSNP	rs28933971
dbSNP (classic)	rs28933971
ClinGen	rs28933971
ebi	rs28933971
HLI	rs28933971
Exac	rs28933971
Gnomad	rs28933971
Varsome	rs28933971
LitVar	rs28933971
Map	rs28933971
PheGenI	rs28933971
Biobank	rs28933971
1000 genomes	rs28933971
hgdp	rs28933971
ensembl	rs28933971
geneview	rs28933971
scholar	rs28933971
google	rs28933971
pharmgkb	rs28933971
gwascentral	rs28933971
openSNP	rs28933971
23andMe	rs28933971
SNPshot	rs28933971
SNPdbe	rs28933971
MSV3d	rs28933971
GWAS Ctlg	rs28933971

Max Magnitude

0

OMIM	167416
Desc	TOOTH AGENESIS, SELECTIVE, 3
Variant	0007
Related	also

ClinVar
Risk	rs28933971(C;C)
Alt	rs28933971(C;C)
Reference	Rs28933971(G;G)
Significance	Pathogenic
Disease	Tooth agenesis
Variation	info
Gene	PAX9
CLNDBN	Tooth agenesis, selective, 3
Reversed	0
HGVS	NC_000014.8:g.37132180G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014783.26,