rs1057520742

Orientation

plus

Stabilized

plus

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

Make rs1057520742(C;T)

Make rs1057520742(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

70027947

Gene

EDA

is a	snp
is	mentioned by
dbSNP	rs1057520742
dbSNP (classic)	rs1057520742
ClinGen	rs1057520742
ebi	rs1057520742
HLI	rs1057520742
Exac	rs1057520742
Gnomad	rs1057520742
Varsome	rs1057520742
LitVar	rs1057520742
Map	rs1057520742
PheGenI	rs1057520742
Biobank	rs1057520742
1000 genomes	rs1057520742
hgdp	rs1057520742
ensembl	rs1057520742
geneview	rs1057520742
scholar	rs1057520742
google	rs1057520742
pharmgkb	rs1057520742
gwascentral	rs1057520742
openSNP	rs1057520742
23andMe	rs1057520742
SNPshot	rs1057520742
SNPdbe	rs1057520742
MSV3d	rs1057520742
GWAS Ctlg	rs1057520742

Max Magnitude

0

ClinVar
Risk	rs1057520742(T;T)
Alt	rs1057520742(T;T)
Reference	Rs1057520742(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	EDA
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.69247797C>T
CLNSRC
CLNACC	RCV000439320.1,