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rs587784222

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784222(-;-)
Make rs587784222(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position152869108
GeneNSDHL
is asnp
is mentioned by
dbSNPrs587784222
ebirs587784222
HLIrs587784222
Exacrs587784222
Varsomers587784222
Maprs587784222
PheGenIrs587784222
hapmaprs587784222
1000 genomesrs587784222
hgdprs587784222
ensemblrs587784222
gopubmedrs587784222
geneviewrs587784222
scholarrs587784222
googlers587784222
pharmgkbrs587784222
gwascentralrs587784222
openSNPrs587784222
23andMers587784222
23andMe allrs587784222
SNP Nexus

SNPshotrs587784222
SNPdbers587784222
MSV3drs587784222
GWAS Ctlgrs587784222
Max Magnitude0
ClinVar
Risk rs587784222(;)
Alt rs587784222(;)
Reference rs587784222(G;G)
Significance Probable-Pathogenic
Disease Child syndrome
Variation info
Gene NSDHL
CLNDBN Child syndrome
Reversed 0
HGVS NC_000023.10:g.152037652delG
CLNSRC
CLNACC RCV000146960.1,