Variant (rsID / SNP)

rs35868297

rs35868297 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALNTL5. Location: chromosome 7, position 151,668,063. The table records no clinical significance for this variant.

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Reference-table entries

GALNTL5Not classified

Variant type: missense_variant
Chromosome / position: 7:151668063
HGVS: NM_145292.4,c.281A>G,p.His94Arg
Allele change: Silent

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.