Variant (rsID / SNP)

rs8115854

rs8115854 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MROH8. Location: chromosome 20, position 35,766,337. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MROH8Not classified

Variant type: missense_variant
Chromosome / position: 20:35766337
HGVS: NM_152503.7,c.1525T>C,p.Ser509Pro
Allele change: Missense_I509T

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.