Variant (rsID / SNP)

rs861204

rs861204 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS12. Location: chromosome 12, position 51,237,816. The table records no clinical significance for this variant.

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Reference-table entries

TMPRSS12Not classified

Variant type: missense_variant
Chromosome / position: 12:51237816
HGVS: NM_182559.3,c.379G>A,p.Ala127Thr
Allele change: Missense_A127T

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.