Variant (rsID / SNP)

rs4951682

rs4951682 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HHAT. Location: chromosome 1, position 210,804,430. The table records no clinical significance for this variant.

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Reference-table entries

HHATNot classified

Variant type: intron_variant
Chromosome / position: 1:210804430
HGVS: NM_001170587.3,c.1393+7416G>A
Allele change: Silent

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.