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Variant (rsID / SNP)

rs3812547

GPSM1

rs3812547 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPSM1. Location: chromosome 9, position 139,252,495. The table records no clinical significance for this variant.

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Reference-table entries

GPSM1Not classified
Variant type
synonymous_variant
Chromosome / position
9:139252495
HGVS
NM_001145638.3,c.1851G>A,p.Pro617Pro
Allele change
Synonymous_P617P

Public references

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