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Variant (rsID / SNP)

rs1138800

PANX1

rs1138800 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PANX1. Location: chromosome 11, position 93,862,493. The table records no clinical significance for this variant.

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Reference-table entries

PANX1Not classified
Variant type
missense_variant
Chromosome / position
11:93862493
HGVS
NM_015368.4,c.15A>C,p.Gln5His
Allele change
Missense_Q5H

Public references

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