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Variant (rsID / SNP)

rs11552301

TMEM175

rs11552301 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM175. Location: chromosome 4, position 946,226. The table records no clinical significance for this variant.

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Reference-table entries

TMEM175Not classified
Variant type
synonymous_variant
Chromosome / position
4:946226
HGVS
NM_032326.4,c.450T>C,p.Ile150Ile
Allele change
Synonymous_I68I

Associated conditions / phenotypes

Synonymous_I68I|Synonymous_I150I

Public references

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