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rs587784383

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784383(A;A)
Make rs587784383(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position74524762
GeneSLC16A2
is asnp
is mentioned by
dbSNPrs587784383
ebirs587784383
HLIrs587784383
Exacrs587784383
Varsomers587784383
Maprs587784383
PheGenIrs587784383
hapmaprs587784383
1000 genomesrs587784383
hgdprs587784383
ensemblrs587784383
gopubmedrs587784383
geneviewrs587784383
scholarrs587784383
googlers587784383
pharmgkbrs587784383
gwascentralrs587784383
openSNPrs587784383
23andMers587784383
23andMe allrs587784383
SNP Nexus

SNPshotrs587784383
SNPdbers587784383
MSV3drs587784383
GWAS Ctlgrs587784383
Max Magnitude0
ClinVar
Risk rs587784383(A;A)
Alt rs587784383(A;A)
Reference rs587784383(G;G)
Significance Probable-Pathogenic
Disease Allan-Herndon-Dudley syndrome
Variation info
Gene SLC16A2
CLNDBN Allan-Herndon-Dudley syndrome
Reversed 0
HGVS NC_000023.10:g.73744597G>A
CLNSRC
CLNACC RCV000147493.1,