Variant (rsID / SNP)

rs61753635

rs61753635 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MARVELD3. Location: chromosome 16, position 71,660,404. The table records no clinical significance for this variant.

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Reference-table entries

MARVELD3Not classified

Variant type: missense_variant
Chromosome / position: 16:71660404
HGVS: NM_001017967.4,c.272G>A,p.Arg91Gln
Allele change: Missense_R91Q

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.