Variant (rsID / SNP)

rs2301721

rs2301721 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOXA7. Location: chromosome 7, position 27,196,113. The table records no clinical significance for this variant.

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Reference-table entries

HOXA7Not classified

Variant type: missense_variant
Chromosome / position: 7:27196113
HGVS: NM_006896.4,c.52G>A,p.Ala18Thr
Allele change: Missense_A18T

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.