Variant (rsID / SNP)

rs2281731

rs2281731 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLIS3. Location: chromosome 9, position 3,855,616. The table records no clinical significance for this variant.

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Reference-table entries

GLIS3Not classified

Variant type: intron_variant
Chromosome / position: 9:3855616
HGVS: NM_001042413.2,c.2473+393G>A
Allele change: Silent

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.