Variant (rsID / SNP)

rs1063646

rs1063646 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSORS1C1. Location: chromosome 6, position 31,107,648. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PSORS1C1Not classified

Variant type: missense_variant
Chromosome / position: 6:31107648
HGVS: NM_014068.3,c.398C>T,p.Pro133Leu
Allele change: Missense_P133L

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.