Variant (rsID / SNP)

rs10769671

rs10769671 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C11ORF42, C11orf42. Location: chromosome 11, position 6,231,731. The table records no clinical significance for this variant.

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Reference-table entries

C11ORF42Not classified

Variant type: missense_variant
Chromosome / position: 11:6231731
HGVS: NM_173525.3,c.724C>T,p.Pro242Ser
Allele change: Missense_P242S

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.