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Variant (rsID / SNP)

rs183827902

RILP

rs183827902 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RILP. Location: chromosome 17, position 1,552,519. The table records no clinical significance for this variant.

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Reference-table entries

RILPNot classified
Variant type
missense_variant
Chromosome / position
17:1552519
HGVS
NM_031430.3,c.404G>A,p.Arg135Gln
Allele change
Missense_R135Q

Public references

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