Variant (rsID / SNP)

rs2795995

rs2795995 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM164. The table records no clinical significance for this variant.

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Reference-table entries

TMEM164Not classified

Variant type: 3_prime_UTR_variant
HGVS: NM_001353851.2,c.*2486G>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.