Variant (rsID / SNP)

rs2072443

rs2072443 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM176B. Location: chromosome 7, position 150,490,376. The table records no clinical significance for this variant.

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Reference-table entries

TMEM176BNot classified

Variant type: missense_variant
Chromosome / position: 7:150490376
HGVS: NM_001362691.2,c.448G>A,p.Ala150Thr
Allele change: Missense_A97T

Associated conditions / phenotypes

Missense_A134T

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.