rs104894468

Orientation

plus

Stabilized

plus

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

Make rs104894468(A;T)

Make rs104894468(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

36663151

Gene	LOC105370455, PAX9

is a	snp
is	mentioned by
dbSNP	rs104894468
dbSNP (classic)	rs104894468
ClinGen	rs104894468
ebi	rs104894468
HLI	rs104894468
Exac	rs104894468
Gnomad	rs104894468
Varsome	rs104894468
LitVar	rs104894468
Map	rs104894468
PheGenI	rs104894468
Biobank	rs104894468
1000 genomes	rs104894468
hgdp	rs104894468
ensembl	rs104894468
geneview	rs104894468
scholar	rs104894468
google	rs104894468
pharmgkb	rs104894468
gwascentral	rs104894468
openSNP	rs104894468
23andMe	rs104894468
SNPshot	rs104894468
SNPdbe	rs104894468
MSV3d	rs104894468
GWAS Ctlg	rs104894468

Max Magnitude

0

OMIM	167416
Desc
Variant	0009
Related	also

ClinVar
Risk	rs104894468(T;T)
Alt	rs104894468(T;T)
Reference	Rs104894468(A;A)
Significance	Pathogenic
Disease	Tooth agenesis
Variation	info
Gene	PAX9
CLNDBN	Tooth agenesis, selective, 3
Reversed	0
HGVS	NC_000014.8:g.37132356A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014785.25,