Variant (rsID / SNP)

rs4462937

rs4462937 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH12. Location: chromosome 3, position 57,414,434. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DNAH12Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:57414434
Cytoband: 3p14.3
HGVS: NM_001366028.2(DNAH12):c.5179T>C (p.Tyr1727His)
Allele change: Missense_Y1727H

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.