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rs587784225

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587784225(-;-)
Make rs587784225(-;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position152868898
GeneNSDHL
is asnp
is mentioned by
dbSNPrs587784225
ebirs587784225
HLIrs587784225
Exacrs587784225
Varsomers587784225
Maprs587784225
PheGenIrs587784225
hapmaprs587784225
1000 genomesrs587784225
hgdprs587784225
ensemblrs587784225
gopubmedrs587784225
geneviewrs587784225
scholarrs587784225
googlers587784225
pharmgkbrs587784225
gwascentralrs587784225
openSNPrs587784225
23andMers587784225
23andMe allrs587784225
SNP Nexus

SNPshotrs587784225
SNPdbers587784225
MSV3drs587784225
GWAS Ctlgrs587784225
Max Magnitude0
ClinVar
Risk rs587784225(;)
Alt rs587784225(;)
Reference rs587784225(T;T)
Significance Pathogenic
Disease Child syndrome
Variation info
Gene NSDHL
CLNDBN Child syndrome
Reversed 0
HGVS NC_000023.10:g.152037442delT
CLNSRC
CLNACC RCV000146967.1,