rs397516654

Orientation

plus

Stabilized

plus

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

Make rs397516654(C;C)

Make rs397516654(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

70035527

Gene

EDA

is a	snp
is	mentioned by
dbSNP	rs397516654
dbSNP (classic)	rs397516654
ClinGen	rs397516654
ebi	rs397516654
HLI	rs397516654
Exac	rs397516654
Gnomad	rs397516654
Varsome	rs397516654
LitVar	rs397516654
Map	rs397516654
PheGenI	rs397516654
Biobank	rs397516654
1000 genomes	rs397516654
hgdp	rs397516654
ensembl	rs397516654
geneview	rs397516654
scholar	rs397516654
google	rs397516654
pharmgkb	rs397516654
gwascentral	rs397516654
openSNP	rs397516654
23andMe	rs397516654
SNPshot	rs397516654
SNPdbe	rs397516654
MSV3d	rs397516654
GWAS Ctlg	rs397516654

Max Magnitude

0

ClinVar
Risk	rs397516654(C;C)
Alt	rs397516654(C;C)
Reference	Rs397516654(T;T)
Significance	Probable-Pathogenic
Disease	Tooth agenesis
Variation	info
Gene	EDA
CLNDBN	Tooth agenesis, selective, X-linked, 1
Reversed	0
HGVS	NC_000023.10:g.69255377T>C
CLNSRC	ClinVar
CLNACC	RCV000037161.2,