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rs387906703

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906703(A;T)
Make rs387906703(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position20195128
GeneRPS6KA3
is asnp
is mentioned by
dbSNPrs387906703
ebirs387906703
HLIrs387906703
Exacrs387906703
Varsomers387906703
Maprs387906703
PheGenIrs387906703
hapmaprs387906703
1000 genomesrs387906703
hgdprs387906703
ensemblrs387906703
gopubmedrs387906703
geneviewrs387906703
scholarrs387906703
googlers387906703
pharmgkbrs387906703
gwascentralrs387906703
openSNPrs387906703
23andMers387906703
23andMe allrs387906703
SNP Nexus

SNPshotrs387906703
SNPdbers387906703
MSV3drs387906703
GWAS Ctlgrs387906703
Max Magnitude0
ClinVar
Risk rs387906703(T;T)
Alt rs387906703(T;T)
Reference rs387906703(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene RPS6KA3
CLNDBN Mental retardation, X-linked 19
Reversed 1
HGVS NC_000023.10:g.20213246T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022823.27,