Variant (rsID / SNP)

rs13169133

rs13169133 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GMCL2. Location: chromosome 5, position 177,612,983. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

GMCL2Not classified

Variant type: missense_variant
Chromosome / position: 5:177612983
HGVS: NM_001358008.2,c.1318C>T,p.Arg440Cys
Allele change: Missense_R440C

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.