Variant (rsID / SNP)

rs28655666

rs28655666 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM120B. Location: chromosome 12, position 122,186,317. The table records no clinical significance for this variant.

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Reference-table entries

TMEM120BNot classified

Variant type: missense_variant
Chromosome / position: 12:122186317
HGVS: NM_001080825.2,c.274G>A,p.Asp92Asn
Allele change: Missense_D92N

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.