Variant (rsID / SNP)

rs7485773

rs7485773 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACSM4, CD163L1. Location: chromosome 12, position 7,475,081. The table records no clinical significance for this variant.

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Reference-table entries

ACSM4Not classified

Variant type: stop_gained
Chromosome / position: 12:7475081
HGVS: NM_001080454.2,c.1069C>T,p.Gln357*
Allele change: Nonsense_Q357X

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.