Variant (rsID / SNP)

rs11196686

rs11196686 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VWA2, AFAP1L2. Location: chromosome 10, position 116,050,008. The table records no clinical significance for this variant.

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Reference-table entries

VWA2Not classified

Variant type: missense_variant
Chromosome / position: 10:116050008
HGVS: NM_001272046.2,c.2132A>G,p.Gln711Arg
Allele change: Missense_Q711R

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.