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rs587784223

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784223(C;T)
Make rs587784223(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position152865870
GeneNSDHL
is asnp
is mentioned by
dbSNPrs587784223
ebirs587784223
HLIrs587784223
Exacrs587784223
Varsomers587784223
Maprs587784223
PheGenIrs587784223
hapmaprs587784223
1000 genomesrs587784223
hgdprs587784223
ensemblrs587784223
gopubmedrs587784223
geneviewrs587784223
scholarrs587784223
googlers587784223
pharmgkbrs587784223
gwascentralrs587784223
openSNPrs587784223
23andMers587784223
23andMe allrs587784223
SNP Nexus

SNPshotrs587784223
SNPdbers587784223
MSV3drs587784223
GWAS Ctlgrs587784223
Max Magnitude0
ClinVar
Risk rs587784223(T;T)
Alt rs587784223(T;T)
Reference rs587784223(C;C)
Significance Probable-Pathogenic
Disease Child syndrome not provided
Variation info
Gene NSDHL
CLNDBN Child syndrome not provided
Reversed 0
HGVS NC_000023.10:g.152034414C>T
CLNSRC
CLNACC RCV000146963.1, RCV000179494.1,