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

rs397515486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515486(C;T)
Make rs397515486(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153964702
GeneHCFC1
is asnp
is mentioned by
dbSNPrs397515486
ebirs397515486
HLIrs397515486
Exacrs397515486
Varsomers397515486
Maprs397515486
PheGenIrs397515486
hapmaprs397515486
1000 genomesrs397515486
hgdprs397515486
ensemblrs397515486
gopubmedrs397515486
geneviewrs397515486
scholarrs397515486
googlers397515486
pharmgkbrs397515486
gwascentralrs397515486
openSNPrs397515486
23andMers397515486
23andMe allrs397515486
SNP Nexus

SNPshotrs397515486
SNPdbers397515486
MSV3drs397515486
GWAS Ctlgrs397515486
Max Magnitude0
ClinVar
Risk rs397515486(T;T)
Alt rs397515486(T;T)
Reference rs397515486(C;C)
Significance Pathogenic
Disease Mental retardation 3 Intellectual disability not provided
Variation info
Gene HCFC1
CLNDBN Mental retardation 3, X-linked Intellectual disability not provided
Reversed 1
HGVS NC_000023.10:g.153230153G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000057507.16, RCV000224133.1, RCV000224484.1,