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rs587784226

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784226(A;A)
Make rs587784226(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position152868900
GeneNSDHL
is asnp
is mentioned by
dbSNPrs587784226
ebirs587784226
HLIrs587784226
Exacrs587784226
Varsomers587784226
Maprs587784226
PheGenIrs587784226
hapmaprs587784226
1000 genomesrs587784226
hgdprs587784226
ensemblrs587784226
gopubmedrs587784226
geneviewrs587784226
scholarrs587784226
googlers587784226
pharmgkbrs587784226
gwascentralrs587784226
openSNPrs587784226
23andMers587784226
23andMe allrs587784226
SNP Nexus

SNPshotrs587784226
SNPdbers587784226
MSV3drs587784226
GWAS Ctlgrs587784226
Max Magnitude0
ClinVar
Risk rs587784226(A;A)
Alt rs587784226(A;A)
Reference rs587784226(C;C)
Significance Pathogenic
Disease Child syndrome
Variation info
Gene NSDHL
CLNDBN Child syndrome
Reversed 0
HGVS NC_000023.10:g.152037444C>A
CLNSRC
CLNACC RCV000146968.1,