Variant (rsID / SNP)

rs1047978

rs1047978 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C21ORF91, C21orf91. Location: chromosome 21, position 19,169,155. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

C21ORF91Not classified

Variant type: missense_variant
Chromosome / position: 21:19169155
HGVS: NM_001100420.2,c.408C>G,p.Asp136Glu
Allele change: Missense_D136E

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.