Variant (rsID / SNP)

rs1136644

rs1136644 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LPP. Location: chromosome 3, position 188,590,446. The table records no clinical significance for this variant.

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Reference-table entries

LPPNot classified

Variant type: synonymous_variant
Chromosome / position: 3:188590446
HGVS: NM_001167671.3,c.1605A>G,p.Arg535Arg
Allele change: Synonymous_R388R

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.