Variant (rsID / SNP)

rs2232108

rs2232108 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to URGCP. Location: chromosome 7, position 43,916,727. The table records no clinical significance for this variant.

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Reference-table entries

URGCPNot classified

Variant type: missense_variant
Chromosome / position: 7:43916727
HGVS: NM_001077663.3,c.2335A>C,p.Met779Leu
Allele change: Silent

Associated conditions / phenotypes

Missense_M736L

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.