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Variant (rsID / SNP)

rs4129190

THNSL2

rs4129190 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to THNSL2. Location: chromosome 2, position 88,472,791. The table records no clinical significance for this variant.

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Reference-table entries

THNSL2Not classified
Variant type
missense_variant
Chromosome / position
2:88472791
HGVS
NM_018271.5,c.122G>A,p.Gly41Glu
Allele change
Missense_G41E

Public references

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