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rs137853131

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853131(A;A)
Make rs137853131(A;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position128345497
GeneSLC27A4
is asnp
is mentioned by
dbSNPrs137853131
ebirs137853131
HLIrs137853131
Exacrs137853131
Varsomers137853131
Maprs137853131
PheGenIrs137853131
hapmaprs137853131
1000 genomesrs137853131
hgdprs137853131
ensemblrs137853131
gopubmedrs137853131
geneviewrs137853131
scholarrs137853131
googlers137853131
pharmgkbrs137853131
gwascentralrs137853131
openSNPrs137853131
23andMers137853131
23andMe allrs137853131
SNP Nexus

SNPshotrs137853131
SNPdbers137853131
MSV3drs137853131
GWAS Ctlgrs137853131
Max Magnitude0
OMIM604194
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853131(A;A)
Alt rs137853131(A;A)
Reference rs137853131(C;C)
Significance Pathogenic
Disease Ichthyosis prematurity syndrome
Variation info
Gene SLC27A4
CLNDBN Ichthyosis prematurity syndrome
Reversed 0
HGVS NC_000009.11:g.131107776C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006098.2,