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rs864321628

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864321628(C;C)
Make rs864321628(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71387393
GeneTAF1
is asnp
is mentioned by
dbSNPrs864321628
ebirs864321628
HLIrs864321628
Exacrs864321628
Varsomers864321628
Maprs864321628
PheGenIrs864321628
hapmaprs864321628
1000 genomesrs864321628
hgdprs864321628
ensemblrs864321628
gopubmedrs864321628
geneviewrs864321628
scholarrs864321628
googlers864321628
pharmgkbrs864321628
gwascentralrs864321628
openSNPrs864321628
23andMers864321628
23andMe allrs864321628
SNP Nexus

SNPshotrs864321628
SNPdbers864321628
MSV3drs864321628
GWAS Ctlgrs864321628
Max Magnitude0
ClinVar
Risk rs864321628(C;C)
Alt rs864321628(C;C)
Reference rs864321628(T;T)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene TAF1
CLNDBN Mental retardation, X-linked, syndromic 33
Reversed 0
HGVS NC_000023.10:g.70607243T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000203551.1,