rs397516657

Orientation

plus

Stabilized

plus

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

Make rs397516657(A;A)

Make rs397516657(A;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

69616472

Gene

EDA

is a	snp
is	mentioned by
dbSNP	rs397516657
dbSNP (classic)	rs397516657
ClinGen	rs397516657
ebi	rs397516657
HLI	rs397516657
Exac	rs397516657
Gnomad	rs397516657
Varsome	rs397516657
LitVar	rs397516657
Map	rs397516657
PheGenI	rs397516657
Biobank	rs397516657
1000 genomes	rs397516657
hgdp	rs397516657
ensembl	rs397516657
geneview	rs397516657
scholar	rs397516657
google	rs397516657
pharmgkb	rs397516657
gwascentral	rs397516657
openSNP	rs397516657
23andMe	rs397516657
SNPshot	rs397516657
SNPdbe	rs397516657
MSV3d	rs397516657
GWAS Ctlg	rs397516657

Max Magnitude

0

ClinVar
Risk	rs397516657(A;A)
Alt	rs397516657(A;A)
Reference	Rs397516657(T;T)
Significance	Probable-Pathogenic
Disease	Hypohidrotic ectodermal dysplasia
Variation	info
Gene	EDA
CLNDBN	Hypohidrotic ectodermal dysplasia
Reversed	0
HGVS	NC_000023.10:g.68836316T>A
CLNSRC	ClinVar
CLNACC	RCV000037164.2,