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Variant (rsID / SNP)

rs137878529

NCF2

rs137878529 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NCF2. Location: chromosome 1, position 183,543,642. Clinical significance in the table: no interpretation for the single variant.

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Reference-table entries

NCF2Other
Clinical significance (as recorded)
no interpretation for the single variant
Variant type
single nucleotide variant
Chromosome / position
1:183543642
Cytoband
1q25.3
HGVS
NM_000433.4(NCF2):c.481A>G (p.Lys161Glu)
Allele change
Missense_K161E

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.