Variant (rsID / SNP)

rs2297539

rs2297539 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SRGAP2. Location: chromosome 1, position 206,603,535. The table records no clinical significance for this variant.

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Reference-table entries

SRGAP2Not classified

Variant type: missense_variant
Chromosome / position: 1:206603535
HGVS: NM_015326.5,c.1261G>A,p.Gly421Ser
Allele change: Missense_G420S

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.