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rs137853133

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853133(C;C)
Make rs137853133(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position128350335
GeneSLC27A4
is asnp
is mentioned by
dbSNPrs137853133
ebirs137853133
HLIrs137853133
Exacrs137853133
Varsomers137853133
Maprs137853133
PheGenIrs137853133
hapmaprs137853133
1000 genomesrs137853133
hgdprs137853133
ensemblrs137853133
gopubmedrs137853133
geneviewrs137853133
scholarrs137853133
googlers137853133
pharmgkbrs137853133
gwascentralrs137853133
openSNPrs137853133
23andMers137853133
23andMe allrs137853133
SNP Nexus

SNPshotrs137853133
SNPdbers137853133
MSV3drs137853133
GWAS Ctlgrs137853133
Max Magnitude0
OMIM604194
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853133(C;C)
Alt rs137853133(C;C)
Reference rs137853133(T;T)
Significance Pathogenic
Disease Ichthyosis prematurity syndrome
Variation info
Gene SLC27A4
CLNDBN Ichthyosis prematurity syndrome
Reversed 0
HGVS NC_000009.11:g.131112614T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006101.2,