Variant (rsID / SNP)

rs7205673

rs7205673 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKD1L2. Location: chromosome 16, position 81,232,275. The table records no clinical significance for this variant.

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Reference-table entries

PKD1L2Not classified

Variant type: missense_variant
Chromosome / position: 16:81232275
HGVS: NM_001076780.2,c.1535C>T,p.Pro512Leu
Allele change: Missense_P512L

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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