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rs587776592

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776592(-;-)
Make rs587776592(-;A)
Make rs587776592(A;A)
ReferenceGRCh38 38.1/142
Chromosome20
Position34413798
GeneITCH
is asnp
is mentioned by
dbSNPrs587776592
ebirs587776592
HLIrs587776592
Exacrs587776592
Varsomers587776592
Maprs587776592
PheGenIrs587776592
hapmaprs587776592
1000 genomesrs587776592
hgdprs587776592
ensemblrs587776592
gopubmedrs587776592
geneviewrs587776592
scholarrs587776592
googlers587776592
pharmgkbrs587776592
gwascentralrs587776592
openSNPrs587776592
23andMers587776592
23andMe allrs587776592
SNP Nexus

SNPshotrs587776592
SNPdbers587776592
MSV3drs587776592
GWAS Ctlgrs587776592
Max Magnitude0
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,