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Variant (rsID / SNP)

rs5996988

MYO18B

rs5996988 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO18B. Location: chromosome 22, position 26,247,456. The table records no clinical significance for this variant.

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Reference-table entries

MYO18BNot classified
Variant type
synonymous_variant
Chromosome / position
22:26247456
HGVS
NM_001318245.2,c.3798G>A,p.Gly1266Gly
Allele change
Synonymous_G1265G

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.