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Variant (rsID / SNP)

rs1446585

R3HDM1

rs1446585 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to R3HDM1. Location: chromosome 2, position 136,407,479. The table records no clinical significance for this variant.

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Reference-table entries

R3HDM1Not classified
Variant type
missense_variant
Chromosome / position
2:136407479
HGVS
NM_001378107.1,c.1631A>G,p.His544Arg
Allele change
Silent

Public references

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