Variant (rsID / SNP)

rs4272850

rs4272850 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM132C. Location: chromosome 12, position 129,153,986. The table records no clinical significance for this variant.

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Reference-table entries

TMEM132CNot classified

Variant type: missense_variant
Chromosome / position: 12:129153986
HGVS: NM_001136103.3,c.1330G>A,p.Val444Ile
Allele change: Missense_V444I

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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