Variant (rsID / SNP)

rs2293172

rs2293172 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GIMAP4. Location: chromosome 7, position 150,269,542. The table records no clinical significance for this variant.

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Reference-table entries

GIMAP4Not classified

Variant type: missense_variant
Chromosome / position: 7:150269542
HGVS: NM_001363532.2,c.426G>T,p.Glu142Asp
Allele change: Missense_E128D

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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