rs121908123

Orientation

plus

Stabilized

plus

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

Make rs121908123(A;A)

Make rs121908123(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

218881022

Gene	LOC107984111, WNT10A

is a	snp
is	mentioned by
dbSNP	rs121908123
dbSNP (classic)	rs121908123
ClinGen	rs121908123
ebi	rs121908123
HLI	rs121908123
Exac	rs121908123
Gnomad	rs121908123
Varsome	rs121908123
LitVar	rs121908123
Map	rs121908123
PheGenI	rs121908123
Biobank	rs121908123
1000 genomes	rs121908123
hgdp	rs121908123
ensembl	rs121908123
geneview	rs121908123
scholar	rs121908123
google	rs121908123
pharmgkb	rs121908123
gwascentral	rs121908123
openSNP	rs121908123
23andMe	rs121908123
SNPshot	rs121908123
SNPdbe	rs121908123
MSV3d	rs121908123
GWAS Ctlg	rs121908123

Max Magnitude

0

OMIM	606268
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121908123(A;A)
Alt	rs121908123(A;A)
Reference	Rs121908123(G;G)
Significance	Pathogenic
Disease	Odontoonychodermal dysplasia
Variation	info
Gene	WNT10A
CLNDBN	Odontoonychodermal dysplasia
Reversed	0
HGVS	NC_000002.11:g.219745744G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004720.2,