Variant (rsID / SNP)

rs10908496

rs10908496 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLMP. Location: chromosome 1, position 156,264,000. The table records no clinical significance for this variant.

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Reference-table entries

GLMPNot classified

Variant type: missense_variant
Chromosome / position: 1:156264000
HGVS: NM_144580.3,c.607C>T,p.Pro203Ser
Allele change: Missense_P122S

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.