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Variant (rsID / SNP)

rs3740779

LRRC32

rs3740779 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRC32. Location: chromosome 11, position 76,372,052. The table records no clinical significance for this variant.

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Reference-table entries

LRRC32Not classified
Variant type
synonymous_variant
Chromosome / position
11:76372052
HGVS
NM_001128922.2,c.585T>C,p.Gly195Gly
Allele change
Synonymous_G195G

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.