Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906501

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCT;TCT) 0 common in clinvar
Make rs387906501(-;-)
Make rs387906501(-;TCT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position74521020
GeneSLC16A2
is asnp
is mentioned by
dbSNPrs387906501
ebirs387906501
HLIrs387906501
Exacrs387906501
Varsomers387906501
Maprs387906501
PheGenIrs387906501
hapmaprs387906501
1000 genomesrs387906501
hgdprs387906501
ensemblrs387906501
gopubmedrs387906501
geneviewrs387906501
scholarrs387906501
googlers387906501
pharmgkbrs387906501
gwascentralrs387906501
openSNPrs387906501
23andMers387906501
23andMe allrs387906501
SNP Nexus

SNPshotrs387906501
SNPdbers387906501
MSV3drs387906501
GWAS Ctlgrs387906501
Max Magnitude0
ClinVar
Risk rs387906501(;)
Alt rs387906501(;)
Reference rs387906501(TCT;TCT)
Significance Other
Disease Allan-Herndon-Dudley syndrome
Variation info
Gene SLC16A2
CLNDBN Allan-Herndon-Dudley syndrome
Reversed 0
HGVS NC_000023.10:g.73740861_73740863delTCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000012407.16,