Variant (rsID / SNP)

rs17018890

rs17018890 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SRGAP2. Location: chromosome 1, position 206,634,429. The table records no clinical significance for this variant.

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Reference-table entries

SRGAP2Not classified

Variant type: missense_variant
Chromosome / position: 1:206634429
HGVS: NM_015326.5,c.2623A>G,p.Arg875Gly
Allele change: Missense_R874G

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.