Variant (rsID / SNP)

rs116803428

rs116803428 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM44. Location: chromosome 3, position 194,338,399. The table records no clinical significance for this variant.

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Reference-table entries

TMEM44Not classified

Variant type: missense_variant
Chromosome / position: 3:194338399
HGVS: NM_001166305.2,c.719C>T,p.Ala240Val
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.