Variant (rsID / SNP)

rs2743201

rs2743201 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAX7. Location: chromosome 1, position 19,027,239. The table records no clinical significance for this variant.

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Reference-table entries

PAX7Not classified

Variant type: synonymous_variant
Chromosome / position: 1:19027239
HGVS: NM_002584.3,c.879A>G,p.Pro293Pro
Allele change: Synonymous_P291P

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.