Variant (rsID / SNP)

rs2298645

rs2298645 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HSBP1L1. Location: chromosome 18, position 77,728,135. The table records no clinical significance for this variant.

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Reference-table entries

HSBP1L1Not classified

Variant type: missense_variant
Chromosome / position: 18:77728135
HGVS: NM_001136180.2,c.165G>T,p.Lys55Asn
Allele change: Missense_K55N

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.