rs387907197

Orientation

plus

Stabilized

plus

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

Make rs387907197(C;T)

Make rs387907197(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

70033430

Gene

EDA

is a	snp
is	mentioned by
dbSNP	rs387907197
dbSNP (classic)	rs387907197
ClinGen	rs387907197
ebi	rs387907197
HLI	rs387907197
Exac	rs387907197
Gnomad	rs387907197
Varsome	rs387907197
LitVar	rs387907197
Map	rs387907197
PheGenI	rs387907197
Biobank	rs387907197
1000 genomes	rs387907197
hgdp	rs387907197
ensembl	rs387907197
geneview	rs387907197
scholar	rs387907197
google	rs387907197
pharmgkb	rs387907197
gwascentral	rs387907197
openSNP	rs387907197
23andMe	rs387907197
SNPshot	rs387907197
SNPdbe	rs387907197
MSV3d	rs387907197
GWAS Ctlg	rs387907197

Max Magnitude

0

ClinVar
Risk	rs387907197(T;T)
Alt	rs387907197(T;T)
Reference	Rs387907197(C;C)
Significance	Pathogenic
Disease	Hypohidrotic X-linked ectodermal dysplasia
Variation	info
Gene	EDA
CLNDBN	Hypohidrotic X-linked ectodermal dysplasia
Reversed	0
HGVS	NC_000023.10:g.69253280C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024599.2,