Variant (rsID / SNP)

rs72779942

rs72779942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO6A1. Location: chromosome 5, position 101,724,472. The table records no clinical significance for this variant.

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Reference-table entries

SLCO6A1Not classified

Variant type: missense_variant
Chromosome / position: 5:101724472
HGVS: NM_001289002.2,c.1937G>A,p.Arg646Gln
Allele change: Missense_R393Q

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.