Variant (rsID / SNP)

rs310453

rs310453 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SBK2. Location: chromosome 19, position 56,047,448. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SBK2Not classified

Variant type: missense_variant
Chromosome / position: 19:56047448
HGVS: NM_001370096.2,c.214T>C,p.Cys72Arg
Allele change: Missense_C72R

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.