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rs137853321

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853321(A;G)
Make rs137853321(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154564460
GeneIKBKG
is asnp
is mentioned by
dbSNPrs137853321
ebirs137853321
HLIrs137853321
Exacrs137853321
Varsomers137853321
Maprs137853321
PheGenIrs137853321
hapmaprs137853321
1000 genomesrs137853321
hgdprs137853321
ensemblrs137853321
gopubmedrs137853321
geneviewrs137853321
scholarrs137853321
googlers137853321
pharmgkbrs137853321
gwascentralrs137853321
openSNPrs137853321
23andMers137853321
23andMe allrs137853321
SNP Nexus

SNPshotrs137853321
SNPdbers137853321
MSV3drs137853321
GWAS Ctlgrs137853321
Max Magnitude0
ClinVar
Risk rs137853321(G;G)
Alt rs137853321(G;G)
Reference rs137853321(A;A)
Significance Pathogenic
Disease Ectodermal dysplasia Incontinentia pigmenti syndrome
Variation info
Gene IKBKG
CLNDBN Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Incontinentia pigmenti syndrome
Reversed 0
HGVS NC_000023.10:g.153792675A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012203.12, RCV000170521.2,