rs1057517882

Orientation

plus

Stabilized

plus

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

Make rs1057517882(C;C)

Make rs1057517882(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

70030496

Gene

EDA

is a	snp
is	mentioned by
dbSNP	rs1057517882
dbSNP (classic)	rs1057517882
ClinGen	rs1057517882
ebi	rs1057517882
HLI	rs1057517882
Exac	rs1057517882
Gnomad	rs1057517882
Varsome	rs1057517882
LitVar	rs1057517882
Map	rs1057517882
PheGenI	rs1057517882
Biobank	rs1057517882
1000 genomes	rs1057517882
hgdp	rs1057517882
ensembl	rs1057517882
geneview	rs1057517882
scholar	rs1057517882
google	rs1057517882
pharmgkb	rs1057517882
gwascentral	rs1057517882
openSNP	rs1057517882
23andMe	rs1057517882
SNPshot	rs1057517882
SNPdbe	rs1057517882
MSV3d	rs1057517882
GWAS Ctlg	rs1057517882

Max Magnitude

0

ClinVar
Risk	rs1057517882(C;C)
Alt	rs1057517882(C;C)
Reference	Rs1057517882(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	EDA
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.69250346G>C
CLNSRC
CLNACC	RCV000413515.1,