Variant (rsID / SNP)

rs144390858

rs144390858 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH7. Location: chromosome 2, position 196,866,433. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DNAH7Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:196866433
Cytoband: 2q32.3
HGVS: NM_018897.3(DNAH7):c.1139T>G (p.Met380Arg)
Allele change: Missense_M380R

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.