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rs137853166

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853166(A;A)
Make rs137853166(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position7334066
GeneSTS
is asnp
is mentioned by
dbSNPrs137853166
ebirs137853166
HLIrs137853166
Exacrs137853166
Varsomers137853166
Maprs137853166
PheGenIrs137853166
hapmaprs137853166
1000 genomesrs137853166
hgdprs137853166
ensemblrs137853166
gopubmedrs137853166
geneviewrs137853166
scholarrs137853166
googlers137853166
pharmgkbrs137853166
gwascentralrs137853166
openSNPrs137853166
23andMers137853166
23andMe allrs137853166
SNP Nexus

SNPshotrs137853166
SNPdbers137853166
MSV3drs137853166
GWAS Ctlgrs137853166
Max Magnitude0
OMIM300747
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853166(A;A)
Alt rs137853166(A;A)
Reference rs137853166(G;G)
Significance Pathogenic
Disease X-linked ichthyosis with steryl-sulfatase deficiency
Variation info
Gene STS
CLNDBN X-linked ichthyosis with steryl-sulfatase deficiency
Reversed 0
HGVS NC_000023.10:g.7252107G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011299.5,