Variant (rsID / SNP)

rs145393322

rs145393322 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VCL. Location: chromosome 10, position 75,867,084. Clinical significance in the table: Uncertain significance.

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Reference-table entries

VCLUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 10:75867084
Cytoband: 10q22.2
HGVS: NM_014000.3(VCL):c.2531C>T (p.Pro844Leu)
Allele change: Missense_P844L

Associated conditions / phenotypes

Dilated cardiomyopathy 1W

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.