Variant (rsID / SNP)

rs7251942

rs7251942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYMPK. Location: chromosome 19, position 46,327,053. The table records no clinical significance for this variant.

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Reference-table entries

SYMPKNot classified

Variant type: synonymous_variant
Chromosome / position: 19:46327053
HGVS: NM_004819.3,c.2571G>A,p.Thr857Thr
Allele change: Synonymous_T857T

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.