Variant (rsID / SNP)

rs7514102

rs7514102 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PROK1. Location: chromosome 1, position 110,998,854. The table records no clinical significance for this variant.

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Reference-table entries

PROK1Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 1:110998854
HGVS: NM_032414.3,c.199G>A,p.Val67Ile
Allele change: Missense_V67I

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.