Variant (rsID / SNP)

rs1683723

rs1683723 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM132C. Location: chromosome 12, position 128,900,005. The table records no clinical significance for this variant.

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Reference-table entries

TMEM132CNot classified

Variant type: missense_variant
Chromosome / position: 12:128900005
HGVS: NM_001136103.3,c.814G>A,p.Val272Ile
Allele change: Missense_V272I

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.