Variant (rsID / SNP)

rs3134605

rs3134605 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPSM3, PBX2. Location: chromosome 6, position 32,159,956. The table records no clinical significance for this variant.

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Reference-table entries

GPSM3Not classified

Variant type: synonymous_variant
Chromosome / position: 6:32159956
HGVS: NM_001276501.2,c.114A>G,p.Pro38Pro
Allele change: Synonymous_P38P

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.