Variant (rsID / SNP)

rs121918727

rs121918727 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGM1. Location: chromosome 14, position 24,729,165. Clinical significance in the table: Pathogenic.

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Reference-table entries

TGM1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 14:24729165
Cytoband: 14q12
HGVS: NM_000359.3(TGM1):c.857G>A (p.Arg286Gln)
Allele change: Missense_R286Q

Associated conditions / phenotypes

Autosomal recessive congenital ichthyosis 1

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.