Variant (rsID / SNP)

rs117715040

rs117715040 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKRD61, EIF2AK1. Location: chromosome 7, position 6,075,760. The table records no clinical significance for this variant.

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Reference-table entries

ANKRD61Not classified

Variant type: missense_variant
Chromosome / position: 7:6075760
HGVS: NM_001271700.2,c.1000C>A,p.Leu334Ile
Allele change: Silent

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.