Variant (rsID / SNP)

rs37973

rs37973 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLCCI1. Location: chromosome 7, position 8,007,876. Clinical significance in the table: drug response.

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Reference-table entries

GLCCI1Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 7:8007876
Cytoband: 7p21.3
HGVS: NM_138426.2(GLCCI1):c.-1106G=
Allele change: Silent

Associated conditions / phenotypes

Glucocorticoid therapy, response to

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.