Variant (rsID / SNP)

rs6836994

rs6836994 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANXA10. Location: chromosome 4, position 169,083,694. The table records no clinical significance for this variant.

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Reference-table entries

ANXA10Not classified

Variant type: missense_variant
Chromosome / position: 4:169083694
HGVS: NM_007193.5,c.211A>C,p.Met71Leu
Allele change: Missense_M71L

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.