Variant (rsID / SNP)

rs11651537

rs11651537 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH17. Location: chromosome 17, position 76,528,790. Clinical significance in the table: Benign.

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Reference-table entries

DNAH17Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:76528790
Cytoband: 17q25.3
HGVS: NM_173628.4(DNAH17):c.2888T>C (p.Ile963Thr)
Allele change: Missense_I963T

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.