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Variant (rsID / SNP)

rs644827

SLC44A4

rs644827 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC44A4. Location: chromosome 6, position 31,838,441. The table records no clinical significance for this variant.

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Reference-table entries

SLC44A4Not classified
Variant type
missense_variant
Chromosome / position
6:31838441
HGVS
NM_025257.3,c.976A>G,p.Met326Val
Allele change
Missense_M250V

Public references

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