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

rs878853259

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853259(A;A)
Make rs878853259(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position24260593
GeneTGM1
is asnp
is mentioned by
dbSNPrs878853259
ebirs878853259
HLIrs878853259
Exacrs878853259
Varsomers878853259
Maprs878853259
PheGenIrs878853259
hapmaprs878853259
1000 genomesrs878853259
hgdprs878853259
ensemblrs878853259
gopubmedrs878853259
geneviewrs878853259
scholarrs878853259
googlers878853259
pharmgkbrs878853259
gwascentralrs878853259
openSNPrs878853259
23andMers878853259
23andMe allrs878853259
SNP Nexus

SNPshotrs878853259
SNPdbers878853259
MSV3drs878853259
GWAS Ctlgrs878853259
Max Magnitude0
ClinVar
Risk rs878853259(A;A)
Alt rs878853259(A;A)
Reference rs878853259(T;T)
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.24729799A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032724.25,