Variant (rsID / SNP)

rs10419363

rs10419363 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SHD. Location: chromosome 19, position 4,280,186. The table records no clinical significance for this variant.

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Reference-table entries

SHDNot classified

Variant type: synonymous_variant
Chromosome / position: 19:4280186
HGVS: NM_001372011.1,c.126C>T,p.Phe42Phe
Allele change: Synonymous_F42F

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.