rs397516672

Orientation

plus

Stabilized

plus

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

Make rs397516672(C;T)

Make rs397516672(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

70029527

Gene

EDA

is a	snp
is	mentioned by
dbSNP	rs397516672
dbSNP (classic)	rs397516672
ClinGen	rs397516672
ebi	rs397516672
HLI	rs397516672
Exac	rs397516672
Gnomad	rs397516672
Varsome	rs397516672
LitVar	rs397516672
Map	rs397516672
PheGenI	rs397516672
Biobank	rs397516672
1000 genomes	rs397516672
hgdp	rs397516672
ensembl	rs397516672
geneview	rs397516672
scholar	rs397516672
google	rs397516672
pharmgkb	rs397516672
gwascentral	rs397516672
openSNP	rs397516672
23andMe	rs397516672
SNPshot	rs397516672
SNPdbe	rs397516672
MSV3d	rs397516672
GWAS Ctlg	rs397516672

Max Magnitude

0

ClinVar
Risk	rs397516672(T;T)
Alt	rs397516672(T;T)
Reference	Rs397516672(C;C)
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.69249377C>T
CLNSRC	ClinVar
CLNACC	RCV000037183.3, RCV000255016.1,