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Variant (rsID / SNP)

rs4819925

GAB4

rs4819925 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GAB4. Location: chromosome 22, position 17,446,991. The table records no clinical significance for this variant.

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Reference-table entries

GAB4Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
22:17446991
HGVS
NM_001037814.1,c.1287G>A,p.Lys429Lys
Allele change
Synonymous_K429K

Public references

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