Variant (rsID / SNP)
rs1671036
rs1671036 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LLGL2. Location: chromosome 17, position 73,552,185. The table records no clinical significance for this variant.
Reference-table entries
LLGL2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:73552185
- HGVS
- NM_001031803.2,c.134G>A,p.Arg45His
- Allele change
- Missense_R45H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.