Variant (rsID / SNP)

rs41286126

rs41286126 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMO7. Location: chromosome 13, position 76,395,464. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LMO7Not classified

Variant type: missense_variant
Chromosome / position: 13:76395464
HGVS: NM_001306080.2,c.2359C>T,p.Pro787Ser
Allele change: Missense_P505S

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.