Variant (rsID / SNP)

rs6960270

rs6960270 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALNTL5. Location: chromosome 7, position 151,680,072. The table records no clinical significance for this variant.

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Reference-table entries

GALNTL5Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 7:151680072
HGVS: NM_145292.4,c.370T>C,p.Cys124Arg
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.