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Variant (rsID / SNP)

rs11237145

GDPD4

rs11237145 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GDPD4. Location: chromosome 11, position 76,954,812. The table records no clinical significance for this variant.

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Reference-table entries

GDPD4Not classified
Variant type
missense_variant
Chromosome / position
11:76954812
HGVS
NM_182833.3,c.1168A>G,p.Ile390Val
Allele change
Missense_I390V

Public references

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