Variant (rsID / SNP)

rs3736890

rs3736890 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MACF1. Location: chromosome 1, position 39,549,983. The table records no clinical significance for this variant.

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Reference-table entries

MACF1Not classified

Variant type: synonymous_variant
Chromosome / position: 1:39549983
HGVS: NM_012090.5,c.93G>A,p.Ser31Ser
Allele change: Synonymous_S31S

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.