rs397516670

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CCTCCAGGTCCTCCTGGTCCTCAAGGACCCCCTGG;CCTCCAGGTCCTCCTGGTCCTCAAGGACCCCCTGG)	0	common in clinvar
(TCCTCCTGGTCCTCAAGGACCCCCTGGCCTCCAGG;TCCTCCTGGTCCTCAAGGACCCCCTGGCCTCCAGG)	0	common in clinvar

Make rs397516670(-;-)

Make rs397516670(-;TCCTCCTGGTCCTCAAGGACCCCCTGGCCTCCAGG)

Reference

GRCh38 38.1/141

Chromosome

X

Position

70027993

Gene

EDA

is a	snp
is	mentioned by
dbSNP	rs397516670
dbSNP (classic)	rs397516670
ClinGen	rs397516670
ebi	rs397516670
HLI	rs397516670
Exac	rs397516670
Gnomad	rs397516670
Varsome	rs397516670
LitVar	rs397516670
Map	rs397516670
PheGenI	rs397516670
Biobank	rs397516670
1000 genomes	rs397516670
hgdp	rs397516670
ensembl	rs397516670
geneview	rs397516670
scholar	rs397516670
google	rs397516670
pharmgkb	rs397516670
gwascentral	rs397516670
openSNP	rs397516670
23andMe	rs397516670
SNPshot	rs397516670
SNPdbe	rs397516670
MSV3d	rs397516670
GWAS Ctlg	rs397516670

Max Magnitude

0

ClinVar
Risk	rs397516670(-;-)
Alt	rs397516670(-;-)
Reference	Rs397516670(CCTCCAGGTCCTCCTGGTCCTCAAGGACCCCCTGG;CCTCCAGGTCCTCCTGGTCCTCAAGGACCCCCTGG)
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.69247843_69247877del35
CLNSRC	ClinVar
CLNACC	RCV000037180.2, RCV000255942.1,