Variant (rsID / SNP)

rs56206226

rs56206226 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C10ORF71, C10orf71. Location: chromosome 10, position 50,531,549. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

C10ORF71Not classified

Variant type: missense_variant
Chromosome / position: 10:50531549
HGVS: NM_001135196.2,c.959G>T,p.Arg320Leu
Allele change: Missense_R320L

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.