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Variant (rsID / SNP)

rs62370437

SLCO4C1

rs62370437 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO4C1. Location: chromosome 5, position 101,575,091. The table records no clinical significance for this variant.

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Reference-table entries

SLCO4C1Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
5:101575091
HGVS
NM_180991.5,c.1878G>A,p.Gly626Gly
Allele change
Synonymous_G626G

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.