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Variant (rsID / SNP)

rs571353

GDPD5

rs571353 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GDPD5. Location: chromosome 11, position 75,152,243. The table records no clinical significance for this variant.

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Reference-table entries

GDPD5Not classified
Variant type
missense_variant
Chromosome / position
11:75152243
HGVS
NM_030792.8,c.1438G>A,p.Ala480Thr
Allele change
Missense_A342T

Public references

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