Variant (rsID / SNP)

rs1861973

rs1861973 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EN2. Location: chromosome 7, position 155,254,145. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

EN2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:155254145
Cytoband: 7q36.3
HGVS: NM_001427.4(EN2):c.686-921T>C
Allele change: Silent

Associated conditions / phenotypes

Autism, susceptibility to, 10

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.