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rs397515487

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515487(A;A)
Make rs397515487(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153964703
GeneHCFC1
is asnp
is mentioned by
dbSNPrs397515487
ebirs397515487
HLIrs397515487
Exacrs397515487
Varsomers397515487
Maprs397515487
PheGenIrs397515487
hapmaprs397515487
1000 genomesrs397515487
hgdprs397515487
ensemblrs397515487
gopubmedrs397515487
geneviewrs397515487
scholarrs397515487
googlers397515487
pharmgkbrs397515487
gwascentralrs397515487
openSNPrs397515487
23andMers397515487
23andMe allrs397515487
SNP Nexus

SNPshotrs397515487
SNPdbers397515487
MSV3drs397515487
GWAS Ctlgrs397515487
Max Magnitude0
ClinVar
Risk rs397515487(A;A)
Alt rs397515487(A;A)
Reference rs397515487(G;G)
Significance Pathogenic
Disease Mental retardation 3
Variation info
Gene HCFC1
CLNDBN Mental retardation 3, X-linked
Reversed 1
HGVS NC_000023.10:g.153230154C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000057508.16,