rs1057521131

Orientation

plus

Stabilized

plus

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

Make rs1057521131(C;C)

Make rs1057521131(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

69957124

Gene

EDA

is a	snp
is	mentioned by
dbSNP	rs1057521131
dbSNP (classic)	rs1057521131
ClinGen	rs1057521131
ebi	rs1057521131
HLI	rs1057521131
Exac	rs1057521131
Gnomad	rs1057521131
Varsome	rs1057521131
LitVar	rs1057521131
Map	rs1057521131
PheGenI	rs1057521131
Biobank	rs1057521131
1000 genomes	rs1057521131
hgdp	rs1057521131
ensembl	rs1057521131
geneview	rs1057521131
scholar	rs1057521131
google	rs1057521131
pharmgkb	rs1057521131
gwascentral	rs1057521131
openSNP	rs1057521131
23andMe	rs1057521131
SNPshot	rs1057521131
SNPdbe	rs1057521131
MSV3d	rs1057521131
GWAS Ctlg	rs1057521131

Max Magnitude

0

ClinVar
Risk	rs1057521131(C;C)
Alt	rs1057521131(C;C)
Reference	Rs1057521131(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	EDA
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.69176974G>C
CLNSRC
CLNACC	RCV000432953.1,