rs766021478

Orientation

plus

Stabilized

plus

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

Make rs766021478(C;T)

Make rs766021478(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

48966479

Gene

WNT10B

is a	snp
is	mentioned by
dbSNP	rs766021478
dbSNP (classic)	rs766021478
ClinGen	rs766021478
ebi	rs766021478
HLI	rs766021478
Exac	rs766021478
Gnomad	rs766021478
Varsome	rs766021478
LitVar	rs766021478
Map	rs766021478
PheGenI	rs766021478
Biobank	rs766021478
1000 genomes	rs766021478
hgdp	rs766021478
ensembl	rs766021478
geneview	rs766021478
scholar	rs766021478
google	rs766021478
pharmgkb	rs766021478
gwascentral	rs766021478
openSNP	rs766021478
23andMe	rs766021478
SNPshot	rs766021478
SNPdbe	rs766021478
MSV3d	rs766021478
GWAS Ctlg	rs766021478

Max Magnitude

0

ClinVar
Risk	rs766021478(T;T)
Alt	rs766021478(T;T)
Reference	Rs766021478(C;C)
Significance	Pathogenic
Disease	Tooth agenesis
Variation	info
Gene	WNT10B
CLNDBN	Tooth agenesis, selective, 8
Reversed	0
HGVS	NC_000012.11:g.49360262C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000239472.1,