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rs587784384

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784384(C;T)
Make rs587784384(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position74525834
GeneSLC16A2
is asnp
is mentioned by
dbSNPrs587784384
ebirs587784384
HLIrs587784384
Exacrs587784384
Varsomers587784384
Maprs587784384
PheGenIrs587784384
hapmaprs587784384
1000 genomesrs587784384
hgdprs587784384
ensemblrs587784384
gopubmedrs587784384
geneviewrs587784384
scholarrs587784384
googlers587784384
pharmgkbrs587784384
gwascentralrs587784384
openSNPrs587784384
23andMers587784384
23andMe allrs587784384
SNP Nexus

SNPshotrs587784384
SNPdbers587784384
MSV3drs587784384
GWAS Ctlgrs587784384
Max Magnitude0
ClinVar
Risk rs587784384(T;T)
Alt rs587784384(T;T)
Reference rs587784384(C;C)
Significance Pathogenic
Disease Allan-Herndon-Dudley syndrome not provided
Variation info
Gene SLC16A2
CLNDBN Allan-Herndon-Dudley syndrome not provided
Reversed 0
HGVS NC_000023.10:g.73745669C>T
CLNSRC
CLNACC RCV000147494.1, RCV000224827.1,