Variant (rsID / SNP)

rs1527263

rs1527263 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSAP. Location: chromosome 7, position 76,991,935. The table records no clinical significance for this variant.

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Reference-table entries

GSAPNot classified

Variant type: missense_variant
Chromosome / position: 7:76991935
HGVS: NM_001350896.2,c.914G>A,p.Gly305Glu
Allele change: Missense_G305E

Associated conditions / phenotypes

Missense_G305E|Missense_G90E|Missense_G305E|Missense_G305E

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.