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rs587784224

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784224(A;A)
Make rs587784224(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position152867611
GeneNSDHL
is asnp
is mentioned by
dbSNPrs587784224
ebirs587784224
HLIrs587784224
Exacrs587784224
Varsomers587784224
Maprs587784224
PheGenIrs587784224
hapmaprs587784224
1000 genomesrs587784224
hgdprs587784224
ensemblrs587784224
gopubmedrs587784224
geneviewrs587784224
scholarrs587784224
googlers587784224
pharmgkbrs587784224
gwascentralrs587784224
openSNPrs587784224
23andMers587784224
23andMe allrs587784224
SNP Nexus

SNPshotrs587784224
SNPdbers587784224
MSV3drs587784224
GWAS Ctlgrs587784224
Max Magnitude0
ClinVar
Risk rs587784224(A;A)
Alt rs587784224(A;A)
Reference rs587784224(G;G)
Significance Probable-Pathogenic
Disease Child syndrome
Variation info
Gene NSDHL
CLNDBN Child syndrome
Reversed 0
HGVS NC_000023.10:g.152036155G>A
CLNSRC
CLNACC RCV000146964.1,