Variant (rsID / SNP)

rs3736918

rs3736918 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HEATR5A. Location: chromosome 14, position 31,819,047. The table records no clinical significance for this variant.

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Reference-table entries

HEATR5ANot classified

Variant type: missense_variant
Chromosome / position: 14:31819047
HGVS: NM_015473.4,c.2656G>A,p.Val886Met
Allele change: Missense_V886M

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.