Variant (rsID / SNP)

rs370241999

rs370241999 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFS7. Location: chromosome 19, position 1,393,225. Clinical significance in the table: Uncertain significance.

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Reference-table entries

NDUFS7Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 19:1393225
Cytoband: 19p13.3
HGVS: NM_024407.5(NDUFS7):c.456-16G>A
Allele change: Silent

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.