Variant (rsID / SNP)

rs1225746

rs1225746 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYCP2L. Location: chromosome 6, position 10,955,408. The table records no clinical significance for this variant.

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Reference-table entries

SYCP2LNot classified

Variant type: missense_variant
Chromosome / position: 6:10955408
HGVS: NM_001040274.3,c.2014C>T,p.Pro672Ser
Allele change: Missense_P672S

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.