Variant (rsID / SNP)

rs7790976

rs7790976 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM178B. Location: chromosome 7, position 140,996,913. The table records no clinical significance for this variant.

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Reference-table entries

TMEM178BNot classified

Variant type: intron_variant
Chromosome / position: 7:140996913
HGVS: NM_001195278.2,c.496+84409G>A
Allele change: Silent

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.