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Variant (rsID / SNP)

rs58237134

TMIGD2

rs58237134 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMIGD2. Location: chromosome 19, position 4,294,623. The table records no clinical significance for this variant.

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Reference-table entries

TMIGD2Not classified
Variant type
missense_variant
Chromosome / position
19:4294623
HGVS
NM_144615.3,c.503G>T,p.Trp168Leu
Allele change
Missense_W168L

Public references

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