Variant (rsID / SNP)

rs62635031

rs62635031 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR143. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

GPR143Not classified

Variant type: single nucleotide variant
Cytoband: Xp22.2
HGVS: NM_000273.3(GPR143):c.353G>A (p.Gly118Glu)
Allele change: Missense_G118E

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.