rs121908122

Orientation

plus

Stabilized

plus

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

Make rs121908122(A;A)

Make rs121908122(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

218893145

Gene

WNT10A

is a	snp
is	mentioned by
dbSNP	rs121908122
dbSNP (classic)	rs121908122
ClinGen	rs121908122
ebi	rs121908122
HLI	rs121908122
Exac	rs121908122
Gnomad	rs121908122
Varsome	rs121908122
LitVar	rs121908122
Map	rs121908122
PheGenI	rs121908122
Biobank	rs121908122
1000 genomes	rs121908122
hgdp	rs121908122
ensembl	rs121908122
geneview	rs121908122
scholar	rs121908122
google	rs121908122
pharmgkb	rs121908122
gwascentral	rs121908122
openSNP	rs121908122
23andMe	rs121908122
SNPshot	rs121908122
SNPdbe	rs121908122
MSV3d	rs121908122
GWAS Ctlg	rs121908122

Max Magnitude

0

OMIM	606268
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121908122(A;A)
Alt	rs121908122(A;A)
Reference	Rs121908122(C;C)
Significance	Pathogenic
Disease	Odontoonychodermal dysplasia
Variation	info
Gene	WNT10A
CLNDBN	Odontoonychodermal dysplasia
Reversed	0
HGVS	NC_000002.11:g.219757867C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004719.2,