Variant (rsID / SNP)

rs2172250

rs2172250 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGSF10, MED12L. Location: chromosome 3, position 151,154,666. The table records no clinical significance for this variant.

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Reference-table entries

IGSF10Not classified

Variant type: synonymous_variant
Chromosome / position: 3:151154666
HGVS: NM_001385060.1,c.7683A>G,p.Thr2561Thr
Allele change: Synonymous_T588T

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.