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Variant (rsID / SNP)

rs11120575

SRGAP2

rs11120575 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SRGAP2. Location: chromosome 1, position 206,626,607. The table records no clinical significance for this variant.

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Reference-table entries

SRGAP2Not classified
Variant type
missense_variant
Chromosome / position
1:206626607
HGVS
NM_015326.5,c.1984G>A,p.Val662Ile
Allele change
Missense_V661I

Public references

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