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Variant (rsID / SNP)

rs2242664

SLC44A4

rs2242664 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC44A4. Location: chromosome 6, position 31,839,331. The table records no clinical significance for this variant.

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Reference-table entries

SLC44A4Not classified
Variant type
synonymous_variant
Chromosome / position
6:31839331
HGVS
NM_025257.3,c.537G>A,p.Gly179Gly
Allele change
Synonymous_G103G

Public references

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