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rs137853323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853323(C;T)
Make rs137853323(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154552186
GeneIKBKG
is asnp
is mentioned by
dbSNPrs137853323
ebirs137853323
HLIrs137853323
Exacrs137853323
Varsomers137853323
Maprs137853323
PheGenIrs137853323
hapmaprs137853323
1000 genomesrs137853323
hgdprs137853323
ensemblrs137853323
gopubmedrs137853323
geneviewrs137853323
scholarrs137853323
googlers137853323
pharmgkbrs137853323
gwascentralrs137853323
openSNPrs137853323
23andMers137853323
23andMe allrs137853323
SNP Nexus

SNPshotrs137853323
SNPdbers137853323
MSV3drs137853323
GWAS Ctlgrs137853323
Max Magnitude0
OMIM300248
Desc
Variant0006
Relatedalso
ClinVar
Risk rs137853323(T;T)
Alt rs137853323(T;T)
Reference rs137853323(C;C)
Significance Pathogenic
Disease Incontinentia pigmenti syndrome
Variation info
Gene IKBKG
CLNDBN Incontinentia pigmenti syndrome
Reversed 0
HGVS NC_000023.10:g.153780401C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012205.12,