Variant (rsID / SNP)

rs144317041

rs144317041 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TIMM44. Location: chromosome 19, position 8,003,040. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TIMM44Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:8003040
Cytoband: 19p13.2
HGVS: NM_006351.4(TIMM44):c.184G>A (p.Gly62Ser)
Allele change: Missense_G62S

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.