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rs137853134

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853134(A;G)
Make rs137853134(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position128352659
GeneSLC27A4
is asnp
is mentioned by
dbSNPrs137853134
ebirs137853134
HLIrs137853134
Exacrs137853134
Varsomers137853134
Maprs137853134
PheGenIrs137853134
hapmaprs137853134
1000 genomesrs137853134
hgdprs137853134
ensemblrs137853134
gopubmedrs137853134
geneviewrs137853134
scholarrs137853134
googlers137853134
pharmgkbrs137853134
gwascentralrs137853134
openSNPrs137853134
23andMers137853134
23andMe allrs137853134
SNP Nexus

SNPshotrs137853134
SNPdbers137853134
MSV3drs137853134
GWAS Ctlgrs137853134
Max Magnitude0
OMIM604194
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853134(G;G)
Alt rs137853134(G;G)
Reference rs137853134(A;A)
Significance Pathogenic
Disease Ichthyosis prematurity syndrome
Variation info
Gene SLC27A4
CLNDBN Ichthyosis prematurity syndrome
Reversed 0
HGVS NC_000009.11:g.131114938A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006102.2,