Variant (rsID / SNP)

rs1003842

rs1003842 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT36. Location: chromosome 17, position 39,646,021. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

KRT36Not classified

Variant type: synonymous_variant
Chromosome / position: 17:39646021
HGVS: NM_003771.5,c.96T>C,p.Arg32Arg
Allele change: Synonymous_R32R

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.