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rs397515485

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515485(C;T)
Make rs397515485(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153964283
GeneHCFC1
is asnp
is mentioned by
dbSNPrs397515485
ebirs397515485
HLIrs397515485
Exacrs397515485
Varsomers397515485
Maprs397515485
PheGenIrs397515485
hapmaprs397515485
1000 genomesrs397515485
hgdprs397515485
ensemblrs397515485
gopubmedrs397515485
geneviewrs397515485
scholarrs397515485
googlers397515485
pharmgkbrs397515485
gwascentralrs397515485
openSNPrs397515485
23andMers397515485
23andMe allrs397515485
SNP Nexus

SNPshotrs397515485
SNPdbers397515485
MSV3drs397515485
GWAS Ctlgrs397515485
Max Magnitude0
ClinVar
Risk rs397515485(G,T;G,T)
Alt rs397515485(G,T;G,T)
Reference rs397515485(C;C)
Significance Pathogenic
Disease Mental retardation 3
Variation info
Gene HCFC1
CLNDBN Mental retardation 3, X-linked
Reversed 1
HGVS NC_000023.10:g.153229734G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000057506.23,