Variant (rsID / SNP)

rs77630516

rs77630516 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HEATR9. Location: chromosome 17, position 34,195,739. The table records no clinical significance for this variant.

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Reference-table entries

HEATR9Not classified

Variant type: missense_variant
Chromosome / position: 17:34195739
HGVS: NM_152781.4,c.8A>G,p.Tyr3Cys
Allele change: Missense_Y3C

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.