Variant (rsID / SNP)

rs1800429

rs1800429 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HEXA. Location: chromosome 15, position 72,643,548. Clinical significance in the table: Uncertain significance.

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Reference-table entries

HEXAUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:72643548
Cytoband: 15q23
HGVS: NM_000520.6(HEXA):c.598G>A (p.Val200Met)
Allele change: Missense_V211M

Associated conditions / phenotypes

Tay-Sachs disease

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.