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Variant (rsID / SNP)

rs2953310

LRRC4C

rs2953310 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRC4C. Location: chromosome 11, position 40,137,543. The table records no clinical significance for this variant.

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Reference-table entries

LRRC4CNot classified
Variant type
synonymous_variant
Chromosome / position
11:40137543
HGVS
NM_001258419.2,c.300A>G,p.Arg100Arg
Allele change
Silent

Public references

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