Variant (rsID / SNP)

rs3735562

rs3735562 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIL. Location: chromosome 7, position 28,996,557. The table records no clinical significance for this variant.

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Reference-table entries

TRILNot classified

Variant type: missense_variant
Chromosome / position: 7:28996557
HGVS: NM_014817.4,c.1103G>A,p.Gly368Asp
Allele change: Missense_A369T

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.