rs397516659

Orientation

plus

Stabilized

plus

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

Make rs397516659(C;C)

Make rs397516659(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

69616310

Gene

EDA

is a	snp
is	mentioned by
dbSNP	rs397516659
dbSNP (classic)	rs397516659
ClinGen	rs397516659
ebi	rs397516659
HLI	rs397516659
Exac	rs397516659
Gnomad	rs397516659
Varsome	rs397516659
LitVar	rs397516659
Map	rs397516659
PheGenI	rs397516659
Biobank	rs397516659
1000 genomes	rs397516659
hgdp	rs397516659
ensembl	rs397516659
geneview	rs397516659
scholar	rs397516659
google	rs397516659
pharmgkb	rs397516659
gwascentral	rs397516659
openSNP	rs397516659
23andMe	rs397516659
SNPshot	rs397516659
SNPdbe	rs397516659
MSV3d	rs397516659
GWAS Ctlg	rs397516659

Max Magnitude

0

ClinVar
Risk	rs397516659(C;C)
Alt	rs397516659(C;C)
Reference	Rs397516659(T;T)
Significance	Pathogenic
Disease	Hypohidrotic ectodermal dysplasia not provided
Variation	info
Gene	EDA
CLNDBN	Hypohidrotic ectodermal dysplasia not provided
Reversed	0
HGVS	NC_000023.10:g.68836154T>C
CLNSRC	ClinVar
CLNACC	RCV000037166.2, RCV000255907.1,