Variant (rsID / SNP)

rs2288649

rs2288649 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IQCA1L. Location: chromosome 7, position 150,888,788. The table records no clinical significance for this variant.

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Reference-table entries

IQCA1LNot classified

Variant type: synonymous_variant
Chromosome / position: 7:150888788
HGVS: NM_001304419.2,c.2283T>C,p.Ser761Ser
Allele change: Missense_L762P

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.