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Variant (rsID / SNP)

rs80114247

TMEM175

rs80114247 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM175. Location: chromosome 4, position 951,791. The table records no clinical significance for this variant.

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Reference-table entries

TMEM175Not classified
Variant type
missense_variant
Chromosome / position
4:951791
HGVS
NM_032326.4,c.1022T>C,p.Met341Thr
Allele change
Missense_M259T

Associated conditions / phenotypes

Missense_M259T|Missense_M341T

Public references

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