Variant (rsID / SNP)

rs11930532

rs11930532 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS11A. Location: chromosome 4, position 68,812,283. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TMPRSS11ANot classified

Variant type: synonymous_variant
Chromosome / position: 4:68812283
HGVS: NM_182606.4,c.18G>A,p.Val6Val
Allele change: Synonymous_V6V

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.