Variant (rsID / SNP)

rs75858661

rs75858661 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRAP. Location: chromosome 21, position 33,678,992. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MRAPBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 21:33678992
Cytoband: 21q22.11
HGVS: NM_001379228.1(MRAP):c.148G>A (p.Val50Met)
Allele change: Missense_V50M

Associated conditions / phenotypes

Glucocorticoid deficiency 2

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.