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Variant (rsID / SNP)

rs1534443

UTRN

rs1534443 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UTRN. Location: chromosome 6, position 144,869,785. The table records no clinical significance for this variant.

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Reference-table entries

UTRNNot classified
Variant type
missense_variant
Chromosome / position
6:144869785
HGVS
NM_007124.3,c.6605A>G,p.Asn2202Ser
Allele change
Missense_N2202S

Public references

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