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Variant (rsID / SNP)

rs1042303

GPLD1

rs1042303 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPLD1. Location: chromosome 6, position 24,437,458. The table records no clinical significance for this variant.

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Reference-table entries

GPLD1Not classified
Variant type
missense_variant
Chromosome / position
6:24437458
HGVS
NM_001503.4,c.2080A>G,p.Met694Val
Allele change
Missense_M694V

Public references

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