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Variant (rsID / SNP)

rs11758242

LY6G5B

rs11758242 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LY6G5B. Location: chromosome 6, position 31,639,845. The table records no clinical significance for this variant.

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Reference-table entries

LY6G5BNot classified
Variant type
missense_variant
Chromosome / position
6:31639845
HGVS
NM_021221.3,c.392C>A,p.Ser131Tyr
Allele change
Missense_S131Y

Public references

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