Variant (rsID / SNP)

rs141922962

rs141922962 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFV3. Location: chromosome 21, position 44,317,156. Clinical significance in the table: Likely benign.

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Reference-table entries

NDUFV3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 21:44317156
Cytoband: 21q22.3
HGVS: NM_021075.4(NDUFV3):c.168A>C (p.Lys56Asn)
Allele change: Missense_K56N

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.