rs146902156

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	3	Likely miscall if from Ancestry data; otherwise, tooth agenesis mutation
(G;G)	0	common in clinvar

Make rs146902156(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

218890256

Gene

WNT10A

is a	snp
is	mentioned by
dbSNP	rs146902156
dbSNP (classic)	rs146902156
ClinGen	rs146902156
ebi	rs146902156
HLI	rs146902156
Exac	rs146902156
Gnomad	rs146902156
Varsome	rs146902156
LitVar	rs146902156
Map	rs146902156
PheGenI	rs146902156
Biobank	rs146902156
1000 genomes	rs146902156
hgdp	rs146902156
ensembl	rs146902156
geneview	rs146902156
scholar	rs146902156
google	rs146902156
pharmgkb	rs146902156
gwascentral	rs146902156
openSNP	rs146902156
23andMe	rs146902156
SNPshot	rs146902156
SNPdbe	rs146902156
MSV3d	rs146902156
GWAS Ctlg	rs146902156

Max Magnitude

3

ClinVar
Risk	Rs146902156(A;A)
Alt	Rs146902156(A;A)
Reference	Rs146902156(G;G)
Significance	Pathogenic
Disease	Tooth agenesis not provided Schopf-Schulz-Passarge syndrome Odontoonychodermal dysplasia Selective tooth agenesis
Variation	info
Gene	WNT10A
CLNDBN	Tooth agenesis, selective, 4 not provided Schopf-Schulz-Passarge syndrome Odontoonychodermal dysplasia Selective tooth agenesis
Reversed	0
HGVS	NC_000002.11:g.219754978G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein) UniProtKB (variants)
CLNACC	RCV000023530.3, RCV000059804.1, RCV000271824.1, RCV000322248.1, RCV000385003.1,

[PMID 21484994] WNT10A and isolated hypodontia.