rs587776592

Orientation

plus

Stabilized

plus

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

Make rs587776592(-;A)

Make rs587776592(A;A)

Reference

GRCh38 38.1/142

Chromosome

20

Position

34413798

Gene

ITCH

is a	snp
is	mentioned by
dbSNP	rs587776592
dbSNP (classic)	rs587776592
ClinGen	rs587776592
ebi	rs587776592
HLI	rs587776592
Exac	rs587776592
Gnomad	rs587776592
Varsome	rs587776592
LitVar	rs587776592
Map	rs587776592
PheGenI	rs587776592
Biobank	rs587776592
1000 genomes	rs587776592
hgdp	rs587776592
ensembl	rs587776592
geneview	rs587776592
scholar	rs587776592
google	rs587776592
pharmgkb	rs587776592
gwascentral	rs587776592
openSNP	rs587776592
23andMe	rs587776592
SNPshot	rs587776592
SNPdbe	rs587776592
MSV3d	rs587776592
GWAS Ctlg	rs587776592

Max Magnitude

0

ClinVar
Risk	rs587776592(A;A)
Alt	rs587776592(A;A)
Reference	Rs587776592(-;-)
Significance	Pathogenic
Disease	Autoimmune disease
Variation	info
Gene	ITCH
CLNDBN	Autoimmune disease, syndromic multisystem
Reversed	0
HGVS	NC_000020.10:g.33001604dupA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004641.3,