Variant (rsID / SNP)

rs11142017

rs11142017 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPATA31E1. Location: chromosome 9, position 90,503,451. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SPATA31E1Not classified

Variant type: missense_variant
Chromosome / position: 9:90503451
HGVS: NM_178828.5,c.4049G>A,p.Arg1350His
Allele change: Silent

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.