Variant (rsID / SNP)

rs2404991

rs2404991 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO7B. Location: chromosome 2, position 128,321,770. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MYO7BNot classified

Variant type: missense_variant
Chromosome / position: 2:128321770
HGVS: NM_001393586.1,c.61G>A,p.Gly21Ser
Allele change: Missense_G21S

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.