Variant (rsID / SNP)

rs12932948

rs12932948 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOC400499. Location: chromosome 16, position 11,544,673. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LOC400499Not classified

Variant type: missense_variant
Chromosome / position: 16:11544673
HGVS: NM_001370704.1,c.4049C>T,p.Ala1350Val

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.