Variant (rsID / SNP)

rs16940665

rs16940665 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LINC02210-CRHR1, CRHR1. Location: chromosome 17, position 43,907,896. The table records no clinical significance for this variant.

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Reference-table entries

LINC02210-CRHR1Not classified

Variant type: synonymous_variant
Chromosome / position: 17:43907896
HGVS: NM_001303016.1,c.366T>C,p.Thr122Thr
Allele change: Synonymous_T48T

Associated conditions / phenotypes

Mental Depression|Depression|Synonymous_T183T

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.