Variant (rsID / SNP)

rs4416743

rs4416743 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INTS15, C7orf26. Location: chromosome 7, position 6,647,738. The table records no clinical significance for this variant.

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Reference-table entries

INTS15Not classified

Variant type: synonymous_variant
Chromosome / position: 7:6647738
HGVS: NM_024067.4,c.1296T>C,p.His432His
Allele change: Synonymous_H432H

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.