Variant (rsID / SNP)

rs2329243

rs2329243 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOC100129307. Location: chromosome 13, position 78,236,720. The table records no clinical significance for this variant.

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Reference-table entries

LOC100129307Not classified

Variant type: non_coding_transcript_exon_variant
Chromosome / position: 13:78236720
HGVS: NR_172722.1,n.42C>T
Allele change: Synonymous_C14C

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.