Variant (rsID / SNP)

rs11680855

rs11680855 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C2ORF92, C2orf92. Location: chromosome 2, position 98,317,685. The table records no clinical significance for this variant.

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Reference-table entries

C2ORF92Not classified

Variant type: missense_variant
Chromosome / position: 2:98317685
HGVS: NM_001351368.2,c.583G>A,p.Ala195Thr
Allele change: Missense_A195T

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.