Variant (rsID / SNP)

rs121918716

rs121918716 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGM1. Location: chromosome 14, position 24,730,985. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

TGM1Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 14:24730985
Cytoband: 14q12
HGVS: NM_000359.3(TGM1):c.424C>T (p.Arg142Cys)
Allele change: Missense_R142C

Associated conditions / phenotypes

Autosomal recessive congenital ichthyosis 1|Lamellar ichthyosis

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.