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Variant (rsID / SNP)

rs6564838

PKD1L2

rs6564838 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKD1L2. Location: chromosome 16, position 81,242,194. The table records no clinical significance for this variant.

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Reference-table entries

PKD1L2Not classified
Variant type
missense_variant
Chromosome / position
16:81242194
HGVS
NM_001076780.2,c.662A>G,p.Glu221Gly
Allele change
Missense_E221G

Public references

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