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Variant (rsID / SNP)

rs1014286

SLC9A4

rs1014286 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC9A4. Location: chromosome 2, position 103,149,100. The table records no clinical significance for this variant.

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Reference-table entries

SLC9A4Not classified
Variant type
missense_variant
Chromosome / position
2:103149100
HGVS
NM_001011552.4,c.2350G>A,p.Gly784Ser
Allele change
Missense_G784S

Public references

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