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rs189437004

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs189437004(A;A)
Make rs189437004(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position123326097
GeneGRIA3
is asnp
is mentioned by
dbSNPrs189437004
ebirs189437004
HLIrs189437004
Exacrs189437004
Varsomers189437004
Maprs189437004
PheGenIrs189437004
hapmaprs189437004
1000 genomesrs189437004
hgdprs189437004
ensemblrs189437004
gopubmedrs189437004
geneviewrs189437004
scholarrs189437004
googlers189437004
pharmgkbrs189437004
gwascentralrs189437004
openSNPrs189437004
23andMers189437004
23andMe allrs189437004
SNP Nexus

SNPshotrs189437004
SNPdbers189437004
MSV3drs189437004
GWAS Ctlgrs189437004
Max Magnitude0
ClinVar
Risk rs189437004(A;A)
Alt rs189437004(A;A)
Reference rs189437004(G;G)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene GRIA3
CLNDBN Mental retardation, X-linked, syndromic, wu type
Reversed 0
HGVS NC_000023.10:g.122459948G>A
CLNSRC
CLNACC RCV000209883.1,