rs121908121

Orientation

plus

Stabilized

plus

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

Make rs121908121(A;A)

Make rs121908121(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

218889990

Gene

WNT10A

is a	snp
is	mentioned by
dbSNP	rs121908121
dbSNP (classic)	rs121908121
ClinGen	rs121908121
ebi	rs121908121
HLI	rs121908121
Exac	rs121908121
Gnomad	rs121908121
Varsome	rs121908121
LitVar	rs121908121
Map	rs121908121
PheGenI	rs121908121
Biobank	rs121908121
1000 genomes	rs121908121
hgdp	rs121908121
ensembl	rs121908121
geneview	rs121908121
scholar	rs121908121
google	rs121908121
pharmgkb	rs121908121
gwascentral	rs121908121
openSNP	rs121908121
23andMe	rs121908121
SNPshot	rs121908121
SNPdbe	rs121908121
MSV3d	rs121908121
GWAS Ctlg	rs121908121

Max Magnitude

0

OMIM	606268
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121908121(A;A)
Alt	rs121908121(A;A)
Reference	Rs121908121(G;G)
Significance	Pathogenic
Disease	Odontoonychodermal dysplasia Tooth agenesis not provided
Variation	info
Gene	WNT10A
CLNDBN	Odontoonychodermal dysplasia Tooth agenesis, selective, 4 not provided
Reversed	0
HGVS	NC_000002.11:g.219754712G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein) UniProtKB (variants)
CLNACC	RCV000004718.3, RCV000030651.3, RCV000059803.1,

[PMID 22581971] Mutations in WNT10A are present in more than half of isolated hypodontia cases.