Have questions? Visit https://www.reddit.com/r/SNPedia

rs398122901

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122901(A;T)
Make rs398122901(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position24262048
GeneTGM1
is asnp
is mentioned by
dbSNPrs398122901
ebirs398122901
HLIrs398122901
Exacrs398122901
Varsomers398122901
Maprs398122901
PheGenIrs398122901
hapmaprs398122901
1000 genomesrs398122901
hgdprs398122901
ensemblrs398122901
gopubmedrs398122901
geneviewrs398122901
scholarrs398122901
googlers398122901
pharmgkbrs398122901
gwascentralrs398122901
openSNPrs398122901
23andMers398122901
23andMe allrs398122901
SNP Nexus

SNPshotrs398122901
SNPdbers398122901
MSV3drs398122901
GWAS Ctlgrs398122901
Max Magnitude0
ClinVar
Risk rs398122901(G,T;G,T)
Alt rs398122901(G,T;G,T)
Reference rs398122901(A;A)
Significance Pathogenic
Disease Autosomal recessive congenital ichthyosis 1
Variation info
Gene TGM1
CLNDBN Autosomal recessive congenital ichthyosis 1
Reversed 1
HGVS NC_000014.8:g.24731254T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032723.25,