Variant (rsID / SNP)

rs1000411

rs1000411 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOC100128988. Location: chromosome 20, position 39,634,616. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LOC100128988Not classified

Variant type: non_coding_transcript_exon_variant
Chromosome / position: 20:39634616
HGVS: NR_145524.1,n.287C>T
Allele change: Silent

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.