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Variant (rsID / SNP)

rs1126682

MRTO4

rs1126682 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRTO4. Location: chromosome 1, position 19,583,636. The table records no clinical significance for this variant.

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Reference-table entries

MRTO4Not classified
Variant type
synonymous_variant
Chromosome / position
1:19583636
HGVS
NM_016183.4,c.270C>T,p.His90His
Allele change
Synonymous_H90H

Public references

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