Variant (rsID / SNP)

rs7212938

rs7212938 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSDMA. Location: chromosome 17, position 38,122,680. The table records no clinical significance for this variant.

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Reference-table entries

GSDMANot classified

Variant type: missense_variant
Chromosome / position: 17:38122680
HGVS: NM_178171.5,c.382G>T,p.Val128Leu
Allele change: Missense_V128L

Associated conditions / phenotypes

Asthma|Ige Responsiveness, Atopic|Childhood-Onset Asthma|Allergic Rhinitis|Rhinitis

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.