Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs34688574

NEURL4

rs34688574 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEURL4. Location: chromosome 17, position 7,220,881. The table records no clinical significance for this variant.

Reference-table entries

NEURL4Not classified
Variant type
missense_variant
Chromosome / position
17:7220881
HGVS
NM_032442.3,c.4217G>A,p.Arg1406His
Allele change
Missense_R1406H

Public references

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