rs28933970

Orientation

plus

Stabilized

plus

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

Make rs28933970(C;C)

Make rs28933970(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

36662954

Gene	LOC105370455, PAX9

is a	snp
is	mentioned by
dbSNP	rs28933970
dbSNP (classic)	rs28933970
ClinGen	rs28933970
ebi	rs28933970
HLI	rs28933970
Exac	rs28933970
Gnomad	rs28933970
Varsome	rs28933970
LitVar	rs28933970
Map	rs28933970
PheGenI	rs28933970
Biobank	rs28933970
1000 genomes	rs28933970
hgdp	rs28933970
ensembl	rs28933970
geneview	rs28933970
scholar	rs28933970
google	rs28933970
pharmgkb	rs28933970
gwascentral	rs28933970
openSNP	rs28933970
23andMe	rs28933970
SNPshot	rs28933970
SNPdbe	rs28933970
MSV3d	rs28933970
GWAS Ctlg	rs28933970

Max Magnitude

0

OMIM	167416
Desc	TOOTH AGENESIS, SELECTIVE, 3
Variant	0005
Related	also

ClinVar
Risk	rs28933970(C;C)
Alt	rs28933970(C;C)
Reference	Rs28933970(T;T)
Significance	Pathogenic
Disease	Tooth agenesis
Variation	info
Gene	PAX9
CLNDBN	Tooth agenesis, selective, 3
Reversed	0
HGVS	NC_000014.8:g.37132159T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014781.26,